Peramelemorphia is an order of marsupials consisting of the bandicoots and bilbies, small to medium-sized, rodent-like mammals characterized by long, pointed snouts, short forelimbs with strong claws for digging, and a rear-opening pouch in females.[1][2] These omnivorous species, which primarily consume insects, small vertebrates, and plant matter, are endemic to Australia, New Guinea, Tasmania, and surrounding islands, inhabiting diverse environments from arid deserts to rainforests.[1][2]The order Peramelemorphia comprises three extant families—Peramelidae (Australian bandicoots, including genera such as Perameles, Isoodon, and Echymipera), Peroryctidae (New Guinean bandicoots, including genera such as Peroryctes and Microperoryctes), and Thylacomyidae (bilbies, genus Macrotis)—along with the extinct family Chaeropodidae, totaling approximately 21 species across 8 genera.[1][2] Members exhibit a stocky build with body masses ranging from under 100 g to over 5 kg, nocturnal habits, and solitary, territorial behavior marked by scent glands; they are agile diggers that create conical foraging pits and burrows.[1]Reproduction is rapid, with short gestation periods of 12.5–14 days, litters of 2–5 young, and females capable of producing up to 16 offspring annually in polygynous or promiscuous mating systems.[1]Phylogenetically, Peramelemorphia occupies a position closely related to dasyuromorphs among Australasian marsupials, with the two groups together sister to diprotodonts, though their polyprotodont dentition and syndactylous hind feet reflect a mosaic of primitive and derived traits.[2] Ecologically, these animals play key roles as insectivores and seed dispersers, serving as prey for predators like dingoes and owls, but many species have declined due to habitat loss, introduced predators, and competition since European settlement.[2][1] As of 2023 IUCN Red List assessments, three species are extinct, four are endangered, and two are vulnerable, underscoring the urgent need for targeted research and protection efforts.[1][3]
Overview
Definition and etymology
Peramelemorphia is an order of Australasian marsupials comprising the bandicoots and bilbies, all of which are endemic to Australia, New Guinea, and surrounding islands. These small to medium-sized, ground-dwelling mammals are distinguished from other marsupials by their polyprotodont dentition, featuring multiple pairs of incisor teeth in both the upper and lower jaws, and syndactylous hind feet, where the second and third toes are fused except at the tips.[1] This unique combination of traits reflects their omnivorous diet and fossorial adaptations, setting them apart within the marsupialclade.The name Peramelemorphia derives from the type genus Perameles, which combines the Ancient Greekpēra (meaning "pouch" or "bag") and Latin meles (meaning "badger" or "marten"), alluding to the animal's marsupial pouch and its badger-like digging habits; the suffix "-morphia" denotes similarity in form.[4] Most members of the order are commonly known as bandicoots, a term originally applied to unrelated large rats in India and derived from the Telugu pandi-kokku ("pig-rat"), later transferred to these marsupials due to their superficial resemblance.[1] The more rabbit-like species in the family Thylacomyidae are specifically called bilbies. These animals are evolutionarily grouped together based on shared anatomical features like syndactyly and polyprotodonty, as well as molecular evidence supporting their monophyly.[1]With approximately 19 living species distributed across three extant families, Peramelemorphia represents a relatively small but ecologically significant order of omnivorous marsupials.[5][6]
Diversity and general distribution
Peramelemorphia encompasses approximately 19 living species divided among three extant families: Peramelidae (with 7 species of bandicoots), Peroryctidae (with 11 species of New Guinean bandicoots), and Thylacomyidae (with 1 species, the greater bilby, Macrotis lagotis). The extinct family Chaeropodidae contributes to a historically higher diversity that included additional genera and species such as the pig-footed bandicoot (Chaeropus ecaudatus). This reduced modern diversity reflects significant losses, particularly in Australia, where at least three species have gone extinct in the last 150 years due to habitat alteration and predation by introduced species.[2][1][6]Members of the order are endemic to Australasia, with their general distribution spanning Australia (including Tasmania), New Guinea, and surrounding islands in the Bismarck Archipelago, as well as historically extending to parts of Wallacea such as Seram and Halmahera in Indonesia. Fossil evidence indicates a broader prehistoric range across these regions, but contemporary populations are fragmented, confined to remnant habitats amid widespread deforestation and agricultural expansion. No native peramelemorph populations exist outside this Australasian realm.[1][7]Endemism patterns highlight greater species diversity in New Guinea, with approximately 12 species—mostly short-nosed bandicoots in the family Peroryctidae adapted to rainforest environments—and some overlap with northern Australian populations such as the northern brown bandicoot (Isoodon macrourus). In Australia, about 8 species occur, particularly in Peramelidae, including the southern brown bandicoot (Isoodon obesulus) and eastern barred bandicoot (Perameles gunnii) in temperate and coastal regions of the south and east, often in fragmented patches. This distribution underscores the order's Gondwanan origins and adaptive radiation across isolated landmasses.[1][6]
Taxonomy
Families and subfamilies
The order Peramelemorphia comprises two extant families: Peramelidae, which includes all living bandicoots, and Thylacomyidae, which consists solely of the bilbies in the genus Macrotis.[2][8] The family Peramelidae is further divided into three subfamilies: Peramelinae (true bandicoots), Echymiperinae (spiny bandicoots), and Peroryctinae (rainforest bandicoots).[9] These subfamilies are distinguished primarily by variations in snout length, ear size, fur texture, and dentition, with Peramelinae featuring shorter snouts and more robust dentition adapted for omnivory, Echymiperinae characterized by spiny pelage and smaller body sizes, and Peroryctinae exhibiting longer snouts suited to forested habitats.[9][7]Extinct families within Peramelemorphia include Chaeropodidae, known for the pig-footed bandicoots with specialized slender limbs for cursorial locomotion, and the more ancient Yaralidae, a Miocene group represented by the genus Yarala and placed in the superfamily Yaraloidea based on cranial morphology.[8][7]At the family level, Peramelidae members are generally short-nosed omnivores with polyprotodont dentition and syndactylous hind feet, adapted for fossorial foraging in diverse habitats, whereas Thylacomyidae are distinguished by their elongated snouts, large rabbit-like ears for heat dissipation and hearing, and burrowing behaviors supported by stronger forelimbs.[2][1]Note that while some recent studies recognize Peroryctidae as a distinct family for New Guinean taxa based on molecular phylogenetics, the prevailing classification treats Peroryctinae and Echymiperinae as subfamilies of Peramelidae.[10]Historically, peramelemorphians were classified within the order Diprotodontia as part of the now-rejected superorder Syndactyla due to superficial similarities in hind foot syndactyly, but molecular and morphological analyses since the early 2000s have firmly established Peramelemorphia as a distinct order within the cohort Marsupialia, sister to Dasyuromorphia and Notoryctemorphia in the clade Agreodontia.[11][12]
Living genera and species
The living members of Peramelemorphia are distributed across two families: Peramelidae and Thylacomyidae, encompassing approximately 20 extant species in seven genera, primarily in Australia and New Guinea.[6] These taxa exhibit a range of body sizes from small, spiny forms to larger, rabbit-like bilbies, with recent genetic analyses refining species boundaries within several genera.[13]
Peramelidae
This family includes the bandicoots, characterized by short to long snouts and omnivorous habits, divided into three subfamilies.
Peramelinae
The Australian bandicoots in this subfamily have shorter snouts. The genus Isoodon comprises four recognized species: the southern brown bandicoot (I. obesulus), northern brown bandicoot (I. macrourus), golden bandicoot (I. auratus), and quenda (I. fusciventer), the latter elevated from subspecies status based on molecular evidence showing closer affinity to I. auratus.[13] The genus Perameles has three extant species: the long-nosed bandicoot (P. nasuta), eastern barred bandicoot (P. gunnii), and western barred bandicoot (P. bougainville), with genetic studies indicating potential further subdivision in the barred bandicoot complex, though currently treated as distinct.[13]
Echymiperinae
Restricted to New Guinea and nearby islands, this subfamily features spiny or small forms adapted to rainforest environments. The genusEchymipera includes five species of spiny bandicoots: Clara's spiny bandicoot (E. clara), David's spiny bandicoot (E. davidi), New Guinean spiny bandicoot (E. echinista), common spiny bandicoot (E. kalubu), and long-nosed spiny bandicoot (E. rufescens).[14] The genusMicroperoryctes has four small species: Papuan bandicoot (M. longicauda), mouse bandicoot (M. murina), Papuan mouse bandicoot (M. papuana), and flat-faced bandicoot (M. platyops).[14]Rhynchomeles is monotypic, represented by the single species Pratt's bandicoot (R. prattorum).[14]
Peroryctinae
Also restricted to New Guinea, this subfamily includes larger, long-snouted forms. The genus Peroryctes contains two species: the giant bandicoot (P. broadbenti) and Tedford's bandicoot (P. tedfordi).[14]
Thylacomyidae
This family is represented solely by the genus Macrotis, with one living species: the greater bilby (M. lagotis), a large, long-eared marsupial with rabbit-like features; the lesser bilby (M. leucura) is considered extinct since the early 20th century.Recent taxonomic revisions, driven by integrated morphological and genetic data since the 2010s, have primarily affected Australian peramelids, such as the recognition of Isoodon fusciventer as a full species in 2018, highlighting the role of molecular phylogenetics in clarifying evolutionary relationships within the order.[13]
Phylogeny
Placement within Marsupialia
Historically, Peramelemorphia was classified within or closely allied to Diprotodontia due to the shared presence of syndactyly, the fusion of the second and third pedal digits, which was interpreted as a synapomorphy suggesting a common ancestry under the group Syndactyla.[15] However, this affinity was challenged by the order's polyprotodont dentition, featuring multiple pairs of incisors typical of more primitive marsupials and aligning it instead with Dasyuromorphia, leading to its recognition as a distinct order by the late 20th century.[15][16]Molecular phylogenetic analyses have solidified Peramelemorphia's position within Australidelphia as part of the Agreodontia clade, sister to Notoryctemorphia, with this pair sister to Dasyuromorphia, outside Diprotodontia. A 2025 retrophylogenomic study using 436 SINE insertions confirms Notoryctemorphia (marsupial moles) as the closest relative to Peramelemorphia.[17][18] The common ancestor of Peramelemorphia and Notoryctemorphia is estimated at approximately 60 million years ago (Paleocene), with the (Peramelemorphia + Notoryctemorphia) clade diverging from Dasyuromorphia around 60–65 million years ago, consistent with refined phylogenomic estimates of 50–60 million years ago for early Agreodontia divergences.[18][19][17] More recent phylogenomic datasets, incorporating fossil calibrations, corroborate this placement and emphasize Peramelemorphia's independent evolutionary trajectory within the post-Cretaceous radiation of Australian marsupials.[19]Morphologically, Peramelemorphia is distinguished by a distinctive blend of primitive and derived traits that set it apart from other marsupial orders, such as Didelphimorphia and Notoryctemorphia.[16] Primitive features include polyprotodont dentition with multiple upper and lower incisors, reflecting an ancestral marsupial condition shared with dasyuromorphs but absent in the single pair of incisors defining diprotodonts. Derived adaptations encompass partial syndactyly of the hind foot digits, which, unlike the complete fusion in Diprotodontia, represents a convergent specialization for locomotion and grooming, further underscoring the order's unique evolutionary niche.[15][16]
Relationships within Peramelemorphia
The phylogenetic relationships within Peramelemorphia reveal a basal divergence of Thylacomyidae, represented by the bilbies (genus Macrotis), which forms the sister group to all other peramelemorphs.[20] This position is supported by morphological traits such as a long, pointed snout and large, upright ears, alongside craniodental features including nasal truncation anterior to the lacrimals and an ossified hypotympanic sinus floor.[20] Molecular analyses, incorporating mitochondrial (e.g., 12S rRNA, cytochrome b, 16S rRNA) and nuclear genes (e.g., ApoB, BRCA1, IRBP, RAG1, vWF), confirm this early split, with divergence estimated at approximately 25–30 million years ago during the late Oligocene to early Miocene.[21]Following the Thylacomyidae, Chaeropodidae—comprising the extinct pig-footed bandicoot (*Chaeropus*)—occupies a stem position relative to the crown-group peramelemorphs, branching off as sister to Peramelidae.[22] This placement resolves earlier uncertainties through total-evidence approaches combining genetic sequences and morphological data, such as the absence of an interparietal bone and polymorphic maxillary fenestrae in *Chaeropus*.[20]Within Peramelidae, the dominant family of bandicoots, Peroryctinae (including New Guinean genera like Peroryctes, Echymipera, and Microperoryctes) represents the basal subfamily, sister to the clade comprising Echymiperinae and Peramelinae.[20] Peroryctinae is characterized by traits like a lacrimal foramen at the maxilla suture and accessory palatal fenestrae in some taxa.[20] Echymiperinae, including Echymipera and related forms, occupies an intermediate position, supported by features such as polymorphic orbitosphenoid exposure and a columelliform stapes.[20] Peramelinae, the derived subfamily, encompasses Australian genera like Isoodon and Perameles, with Isoodon forming the sister group to Perameles.[21] Shared synapomorphies in Peramelinae include pterygoids extending to the carotid canal, a bifid jugal, and a concave stapedial footplate.[20]These relationships are derived from integrated phylogenies that combine molecular data (e.g., ~24.5 kb of concatenated nuclear and mitochondrial sequences) with morphological evidence from dentition (e.g., polyprotodont patterns) and skull structure (e.g., 180 craniodental characters scored across 97 recent and 42 fossil taxa).[20] Recent studies, such as comprehensive craniodental analyses in 2022, have refined these patterns by incorporating total-evidence dating and resolving the stem placement of Chaeropodidae, addressing prior conflicts between molecular and morphological datasets.[20]
Characteristics
Physical morphology
Members of the order Peramelemorphia exhibit a distinctive body plan characterized by a compact, stocky build with a short neck and an arched back, typically resulting in a plump appearance.[1] Body sizes vary across species, ranging from approximately 200 g in smaller forms like the Shark Bay bandicoot to up to 2.5 kg in larger ones such as the greater bilby, with most species weighing around 1 kg.[23][1] A prominent feature is the long, pointed snout, which tapers delicately and is adapted for probing, paired with large, upright ears that range from rounded and small in some bandicoots to prominently elongated and pinkish in bilbies.[1][24] The legs are relatively long and thin, particularly the hind limbs, which are more elongated than the forelimbs, supporting a tapering tail that is short in most bandicoots but longer and brush-like in the bilby.[1][25]Dentition in Peramelemorphia is polyprotodont, featuring multiple pairs of incisors—typically 4 to 5 in the upper jaw and 3 in the lower per side—along with sharp canines for tearing and broad, grinding molars suited to an omnivorous diet.[1] The dental formula generally follows I 4-5/3, C 1/1, P 3/3, M 4/4, totaling 46 to 48 teeth, with narrow, pointed premolars facilitating a mix of shearing and crushing functions.[1] Variations occur across taxa; for instance, the greater bilby possesses 48 teeth with 5 upper incisors and a bifid lower third incisor, reflecting slight reductions or modifications in tooth morphology compared to some bandicoot relatives.[26][27]The limbs and feet display specialized adaptations, with forelimbs shorter and equipped with strong, flat claws on the second, third, and fourth digits for digging, while the first and fifth toes are reduced or absent.[1] Hind feet feature syndactyly, where the second and third toes are fused along their length but retain separate claws, aiding in efficient movement; the fourth toe is the largest.[1] Pelage varies from coarse, short fur in most bandicoots, often brownish or tan with possible stripes, to softer, silkier coats in bilbies, which are blue-grey with rufous tinges on the flanks and white underparts.[1][24]
Locomotion and sensory adaptations
Peramelemorphians, including bandicoots and bilbies, exhibit a distinctive half-bound gait characterized by alternating movements of the fore and hind limbs, where the hindlimbs provide primary propulsion through powerful leaps and hops adapted for navigating brushy or open terrains.[1] This locomotion relies on elongated, robust hindlimbs that enable rapid acceleration, such as during predator evasion via a fast gallop, while the shorter forelimbs are specialized for scratching and digging rather than sustained running.[1] In bilbies (Macrotis spp.), these adaptations extend to deep burrowing, with elongated forelimbs and strong claws facilitating the excavation of extensive spiral burrows up to 3 meters long, supporting both foraging and shelter construction in arid environments.[28]Forelimb musculature in species like the southern brown bandicoot (Isoodon obesulus) features enlarged elbow extensors (over 25% of forelimb mass) and robust attachments for the triceps and pectoral muscles, enhancing mechanical advantage for rapid, shallow digs into soil for invertebrates.[28]Sensory adaptations in Peramelemorphia emphasize nocturnal foraging, with acute olfaction facilitated by a long, pointed snout that detects buried prey and chemical cues from up to several meters away, compensating for limited visual acuity.[1] Vision is adapted for low-light conditions through large eyes suited to dim environments, though it remains secondary to other senses in most species.[1] Hearing is particularly enhanced in open or arid habitats, where large pinnae and expanded tympanic bullae (e.g., in bilbies) improve detection of low-frequency sounds from predators or insects over distances, with bulla size negatively correlating with precipitation levels across taxa.[29] For instance, arid-dwelling bilbies possess the largest relative ear structures among peramelemorphians, aiding in pinpointing subterranean food sources and evading threats at night.[30] These features blend primitive marsupial traits, such as cursorial hindlimbs for bounding, with derived specializations like enlarged auditory bullae in xeric-adapted lineages, optimizing survival in diverse Australian and New Guinean habitats.
Ecology and Behavior
Habitat preferences
Peramelemorphia occupy a diverse array of habitats across Australia, New Guinea, Tasmania, and surrounding islands, reflecting their adaptability as a group. Australian species, such as the greater bilby (Macrotis lagotis), are predominantly found in arid and semi-arid regions, including deserts, spinifex grasslands, and shrublands with sparse ground cover, particularly in central and western Australia like the Tanami Desert and Gibson Desert.[30] In contrast, many peramelid bandicoots prefer more mesic environments; for instance, the southern brown bandicoot (Isoodon obesulus) inhabits coastal heathlands, woodlands, and forests in southern Australia, while the northern brown bandicoot (Isoodon macrourus) occurs in grassy woodlands, heaths, and eucalypt forests in northern and eastern regions.[1][31] New Guinean peroryctines, such as the common echymipera (Echymipera kalubu), extend into tropical rainforests, lowland savannas, and subalpine grasslands, showcasing a broader climatic tolerance within the order.Microhabitat selection emphasizes substrates conducive to their fossorial lifestyle, with a strong preference for friable, sandy, or loamy soils that facilitate burrowing and foraging. Species like the southern brown bandicoot favor sandy or friable soils in heath and open forests, avoiding compacted or heavy clay substrates that hinder digging.[32] Bilbies similarly select sandier, well-aerated soils in arid zones for constructing extensive burrow systems, which can exceed 3 meters in depth.[30] Waterlogged or poorly drained areas are generally unsuitable due to the physical demands of excavation, though some coastal species tolerate moist gullies within otherwise drier habitats. Altitudinal distribution varies significantly; Australian taxa are mostly at low elevations, whereas New Guinean species range from sea level in lowland rainforests to montane forests above 2000 meters, as seen in the mouse bandicoot (Microperoryctes longicauda).[1][14]Contemporary distribution patterns are highly fragmented, largely attributable to anthropogenichabitat modification, resulting in isolated populations rather than continuous ranges. In Australia, many species are now restricted to southwestern and northeastern refugia, such as the southern brown bandicoot (endangered under Australia's EPBC Act) in high-rainfall coastal pockets of Western Australia and Victoria.[33][34][35] New Guinean peroryctines exhibit similar fragmentation, with highland species like Raffray's bandicoot (Peroryctes raffrayana) confined to eastern provincial forests and lowlanders in patchy savannas, exacerbated by agricultural expansion.[36] This discontinuity underscores the order's vulnerability to landscape alterations, though core preferences for diggable soils and vegetative cover persist across taxa.[1]
Diet and foraging strategies
Peramelemorphia exhibit an omnivorous and opportunistic diet, with invertebrates such as insects, grubs, and worms forming the majority of intake in most species, often comprising over 70% of the diet based on faecal analyses.[37] For example, in the long-nosed bandicoot (Perameles nasuta), invertebrate remains dominate scats year-round, including beetles, ants, spiders, and lepidopteran larvae.[37] This is supplemented by plant material like roots, seeds, fungi, and occasionally small vertebrates such as lizards or eggs, allowing adaptation to variable resource availability. In bilbies (Macrotis spp.), the diet similarly emphasizes invertebrates, with beetles occurring in over 80% of scats, termites in 48%, and ants in 40%, though they incorporate a higher proportion of underground plant matter including bulbs and seeds compared to bandicoots.[38]Foraging occurs primarily at night, utilizing their elongated snout and strong foreclaws to probe and excavate soil for subterranean prey. Bandicoots typically create shallow digging pits (up to 10 cm deep) to access insects and fungi, while bilbies dig deeper burrows (often exceeding 20 cm) to reach termite mounds and tubers, reflecting adaptations in forelimb musculature for efficient soil turnover.[39] These activities enhance soil aeration and nutrient cycling in their habitats. Seasonal shifts influence foraging priorities; for instance, long-nosed bandicoots consume more surface invertebrates like orthopterans in summer when availability peaks, shifting to subterranean items such as cicada larvae, roots, and hypogeous fungi in winter when above-ground prey declines.[37] In arid regions, bilbies increase reliance on moisture-rich bulbs during dry periods to supplement water intake.[40]Their digestive system supports this varied omnivory through a relatively simple and short gastrointestinal tract, with the small intestine accounting for at least half the total length to enable rapid processing of protein-rich invertebrate prey. A small caecum, continuous with the proximal colon in some species like the bilby, facilitates limited microbial fermentation of plant fibers, though it is far less developed than in specialized herbivores, prioritizing quick digesta passage over extensive breakdown. This morphology allows selective retention of nutrients from mixed diets, with digestibility varying by food type—higher for insects than fibrous plants—but overall efficiency suits their opportunistic lifestyle.[41]
Social structure and activity patterns
Members of Peramelemorphia, including bandicoots and the greater bilby (Macrotis lagotis), exhibit predominantly solitary social structures, with individuals maintaining separate territories that overlap minimally outside of brief mating interactions.[1] Males typically possess larger home ranges that encompass those of several females, leading to occasional hostile encounters such as chasing or fighting when territories are defended, though territoriality is reduced outside breeding periods.[1] In bandicoots, such as the southern brown bandicoot (Isoodon obesulus), adults are territorial and interact primarily during mating, with females raising young alone in nests or burrows.[42] The greater bilby shows slightly more flexibility, occasionally sharing burrows with opposite-sex individuals or tolerating transient associations, particularly in reinforced populations where males prefer proximity to females, though overall gregariousness remains limited and kin avoidance is evident at shared sites.[43] Complex burrow systems constructed by bilbies may facilitate occasional social tolerance but do not indicate stable groups.[43]Activity patterns in Peramelemorphia are strictly nocturnal or crepuscular, with individuals emerging from nests or burrows at dusk to forage and returning before dawn to avoid diurnal predators.[1]Bandicoots are active for approximately 6-7 hours per night, primarily running and digging within their home ranges, which vary by species and habitat—females typically occupy 1-4 hectares, while males may range over 18-40 hectares in open environments.[42] Some species, like the southern brown bandicoot, employ daily torpor during the day, lowering body temperature to around 33°C to conserve energy in variable climates, with a pronounced circadian rhythm showing peaks in activity at twilight.[44] Home range sizes adjust with resource availability, remaining smaller (e.g., 1-3 hectares for females) in denser habitats.[45]Communication among peramelemorphs relies heavily on olfactory cues rather than elaborate vocal or visual signals, reflecting their solitary and nocturnal lifestyles.[46] Scent marking occurs via glands located posterior to the ears, used by both sexes to delineate territories or signal during encounters; males often rub these glands on vegetation or substrate to assert dominance.[1] Vocalizations are subtle and low-intensity, including puffing calls as warnings and soft spitting or grunting noises during close-range interactions, with no evidence of complex hierarchies or songs.[1] In bilbies, scent from ear glands similarly communicates territorial boundaries, primarily between males, while burrow sharing may involve indirect olfactory recognition without overt aggression.[43]
Reproduction and life history
Peramelemorphia exhibit a polyestrous breeding system, with females capable of multiple cycles per year in favorable conditions, though breeding may become seasonal in temperate regions due to environmental cues.[47]Gestation periods are among the shortest of any mammal, typically lasting 12-14 days, enabling rapid reproduction.[1] Litter sizes range from 1 to 5 young, with females potentially producing up to 4 litters annually, supporting high fecundity in species like the northern brown bandicoot (Isoodon macrourus).[47]Unlike most marsupials, which rely primarily on a choriovitelline placenta, peramelemorphians develop a rudimentary but functional chorioallantoic placenta during gestation, complete with an umbilicus that connects the fetus to the uterine wall.[47] This structure, which forms a discoidal placenta in later stages, supplements nutrient exchange alongside the dominant yolk-sac (choriovitelline) placenta, representing an evolutionary innovation within Marsupialia.[35] The chorioallantoic placenta is resorbed prior to birth, after which the altricial young migrate to the pouch.[48]Newborn young are highly underdeveloped, weighing less than 1 gram, and immediately crawl into the mother's backward-facing pouch to attach to a teat, where they remain for 50-80 days depending on the species.[1] For example, in the long-nosed bandicoot (Perameles nasuta), pouch life averages 50 days, followed by weaning at approximately 2-3 months when young begin independent foraging.[47]Sexual maturity is reached early, at 4-12 months of age, with females maturing slightly faster than males; wild lifespan typically ranges from 2-7 years, influenced by predation and habitat quality.[49]Parental care is provided solely by females, who carry pouch young during the initial development phase and later construct nests for weaned offspring, fostering brief maternal protection without male involvement after mating.[47] This minimal investment aligns with the order's high reproductive output and solitary lifestyle, where young achieve independence soon after weaning.[48]
Conservation
Current status of species
Peramelemorphia encompasses 19 living species, of which approximately 42% (8 species) face conservation challenges according to the IUCN Red List, classified as threatened (Vulnerable or Endangered), with several others rated as Near Threatened or Data Deficient. For instance, the greater bilby (Macrotis lagotis) is listed as Vulnerable, the golden bandicoot (Isoodon auratus) as Endangered, and the lesser bilby (Macrotis leucura) as Extinct, reflecting severe declines across the order.[1]Population estimates for many species remain imprecise due to their elusive nature and remote habitats, but available data indicate critically low numbers for several Australian taxa. The greater bilby, for example, has an estimated total population of around 3,330 individuals across monitored protected areas as of the 2025 Australian Wildlife Conservancy Bilby Census, though mature individuals likely number fewer than 2,500, with ongoing declines observed in non-protected regions.[50][51] New Guinean species, such as those in the genera Echymipera and Peroryctes, appear more stable but are largely Data Deficient, with limited surveys suggesting relative abundance compared to Australian counterparts, though comprehensive data are lacking.Regional patterns highlight greater imperilment among Australian species compared to those in New Guinea and surrounding islands, where habitat fragmentation is less severe. Australian endemics like the greater bilby and golden bandicoot have contracted to less than 20% of their historical ranges, driven by cumulative pressures. Recent assessments in the 2020s have noted ongoing threats for several taxa, attributed to accelerated habitat loss from events like bushfires and land clearing. In contrast, New Guinean populations show slower decline rates, with many classified as Data Deficient but not exhibiting the acute fragmentation seen in Australia.[1][52]
Major threats and conservation measures
Peramelemorphia species face significant anthropogenic pressures that have contributed to the decline of many taxa across their range in Australia and New Guinea. Habitat destruction, primarily driven by agricultural expansion, grazing, mining, and infrastructure development, fragments and degrades essential foraging and shelter sites, reducing available resources and increasing vulnerability to other threats. Altered fire regimes, often intensified by land management for agriculture and pastoralism, lead to more frequent and severe burns that destroy vegetation cover and food sources critical for bandicoots and bilbies. Predation by introduced species such as European red foxes (Vulpes vulpes), feral cats (Felis catus), and wild canids poses a primary threat, with studies showing foxes and cats causing local extinctions and limiting population recovery in affected areas. Competition from invasive herbivores like European rabbits (Oryctolagus cuniculus) and livestock further exacerbates habitat degradation by overgrazing and altering soil structure, while diseases including trypanosomiasis—detected in up to 38% of southern brown bandicoots (Isoodon obesulus) in Tasmania—can impact health and survival, though not yet a dominant factor. Climate change compounds these issues by increasing aridity, extreme temperatures, and erratic rainfall, which may reduce food availability and intensify drought effects on already stressed populations.Conservation efforts for Peramelemorphia emphasize targeted interventions to mitigate these threats. In Australia, protected areas and predator-free zones, such as fenced reserves at Arid Recovery and Mallee Cliffs National Park, provide safe havens where populations can rebound without predation pressure. The 2025 Bilby Census highlighted record growth in several sites, with numbers soaring in areas like Mallee Cliffs. Captive breeding and reintroduction programs, notably for the greater bilby (Macrotis lagotis) since the 1990s, have released thousands of individuals into managed sites, with facilities like Monarto Zoo supporting genetic diversity maintenance. Legal protections under the Environment Protection and Biodiversity Conservation (EPBC) Act 1999 classify many species as vulnerable or endangered, mandating impact assessments and recovery planning to prevent further habitat loss. In New Guinea, community-based monitoring by indigenous groups in conservation areas like the Tonda Wildlife Management Area helps track populations and enforce hunting restrictions, fostering local stewardship amid ongoing habitat pressures.These measures have yielded notable successes, including population recoveries in fenced Australian reserves—for instance, greater bilby numbers growing substantially on islands like Thistle Island following reintroductions—demonstrating the efficacy of predator exclusion. However, challenges persist, particularly with controlling invasive species across vast, remote landscapes, where incomplete eradication allows reinvasion, and climate-driven aridity continues to hinder long-term viability. Ongoing collaboration between governments, indigenous rangers, and organizations like the Save the Bilby Fund remains essential to address these gaps and sustain progress.[50]
Fossil Record
Evolutionary timeline
The evolutionary history of Peramelemorphia traces back to the late Oligocene, approximately 25–30 million years ago, when basal members of the group first appeared in Australia following the dispersal of early marsupials from South America across Antarctica during the early Tertiary (Paleocene to Eocene), approximately 55–65 million years ago.[53][54] This dispersal occurred via land connections between South America, Antarctica, and Australia during the breakup of Gondwana, allowing marsupial lineages to colonize the isolated Australian continent, where Peramelemorphia subsequently evolved in isolation.[55] While the confirmed earliest fossils date to the late Oligocene, potential undescribed early Eocene specimens suggest an even older origin.[53] The earliest fossils, such as those from the Etadunna Formation in South Australia, indicate that these initial forms were small, primitive bandicoot-like marsupials adapted to forested environments.[53]By the early Miocene, around 20 million years ago, basal peramelemorphs had diversified, with molecular estimates placing the origin of the crown group within this period.[56] A significant phase of diversification occurred during the Miocene, particularly between 15 and 20 million years ago, as evidenced by abundant stem forms preserved in the Riversleigh World Heritage Area fossils in northwestern Queensland, reflecting adaptation to a range of habitats amid Australia's ongoing aridification.[57] The middle Miocene, approximately 15–5 million years ago, marked the emergence of key lineages, including Thylacomyidae (the family containing bilbies), which appeared alongside early peramelids in middle Miocene deposits.[58][56]During the Pliocene and Pleistocene, from about 5 million years ago to 11,700 years ago, modern peramelemorph taxa began to emerge, with genera resembling extant bandicoots and bilbies becoming prominent in the fossil record.[53] This period saw a peak in diversity, particularly in the Pleistocene, as the group adapted to increasingly variable climates and ecosystems across Australia.[56] However, declines followed, culminating in significant Holocene extinctions starting around 50,000 years ago, coinciding with human arrival and associated environmental changes, which led to the loss of several species and a contraction of ranges for survivors.[59]
Key extinct taxa and discoveries
One of the most significant fossil sites for Peramelemorphia is the Riversleigh World Heritage Area in northwestern Queensland, Australia, which has yielded Miocene and Pliocene deposits containing numerous extinct bandicoot-like taxa, providing insights into early diversification and morphological evolution.[60] Fossils from this karstic limestone system, dating from the late Oligocene to middle Miocene, include well-preserved skulls and postcrania that reveal primitive features absent in modern forms.[57] The site's exceptional preservation has allowed for detailed studies of dental and skeletal adaptations, highlighting shifts from insectivorous to more omnivorous diets in early peramelemorphians.[53]Yarala burchfieldi, described from a partial skull and jaw fragments at Riversleigh in the Oligo-Miocene, represents one of the oldest and most primitive peramelemorphians, belonging to the extinct family Yaralidae.[61] This small, mouse-sized taxon (approximately the size of a modern antechinus) exhibits primitive syndactyly, with the second and third hind toes fused, a feature linking it to dasyuromorphs and underscoring its basal position in peramelemorphian evolution.[61] Its dentition, intermediate between dasyurids and crown-group bandicoots, suggests an insectivorous diet, and its discovery in 1995 marked the first Miocene peramelemorphian record, extending the group's known antiquity.[53]Galadi speciosus, another Riversleigh find from the Oligo-Miocene, is a short-snouted, dasyuromorph-like bandicoot known from a nearly complete skull and associated postcrania, indicating agile, carnivorous habits similar to modern quolls.[57] Described in 2010, this species, part of the genus Galadi, shows a mix of plesiomorphic traits like a complete centrocrista on molars and apomorphic features such as enlarged auditory bullae, positioning it outside the crown group Peramelemorphia as a stem taxon.[57] Its robust build and large canines imply predation on small vertebrates and insects, contributing to understanding early ecological roles in Australian forests.[62]The genus Bulungu encompasses several robust Miocene species from Riversleigh and the Lake Eyre Basin, such as Bulungu muirheadae and Bulungu palara, characterized by heavy dentaries and molars adapted for crushing tougher vegetation or invertebrates.[53] These taxa, dating to the late Oligocene to early Miocene, represent stem peramelemorphians with body masses around 130-500 grams, filling niches as generalized omnivores in diverse habitats.[63] Their fossils, including isolated teeth and jaw fragments, indicate a radiation of larger-bodied forms before the dominance of smaller, specialized bandicoots.[64]Chaeropus ecaudatus, the pig-footed bandicoot, is a distinctive Holocene taxon known from subfossil remains across arid Australia, including the Lake Eyre Basin and Victoria Cave in South Australia, where it persisted until extinction in the late 1950s.[65] This species featured highly specialized, hoof-like feet with reduced digits, enabling rapid, bounding locomotion suited to open grasslands, a morphology unique among marsupials.[66] Its disappearance, linked to habitat alteration from European settlement, fire regime changes, and introduced predators, highlights vulnerability in arid-adapted peramelemorphians.[65]Recent discoveries from the 2010s, such as Madju variae from Oligo-Miocene Riversleigh deposits, have revealed the first evidence of sexual dimorphism in fossil peramelemorphians, with males exhibiting larger premolars (P3) and overall cranial robusticity compared to females.[67] Described in 2014, this species' ontogenetic series documents growth patterns, suggesting dimorphism related to sexual competition or dietary differences, paralleling patterns in extant peramelids.[67] These finds, alongside Pleistocene assemblages from the Lake Eyre Basin showing diverse bandicoot communities, inform extinction patterns, indicating diet shifts toward aridity tolerance but ultimate decline due to anthropogenic pressures.[53] Victoria Cave's Holocene subfossils, including Chaeropus and other peramelemorphians, further illustrate late survival in refugia before widespread extirpation.[68]