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Macroderma gigas
Captive specimen hanging at roost
Scientific classification Edit this classification
Kingdom: Animalia
Phylum: Chordata
Class: Mammalia
Order: Chiroptera
Family: Megadermatidae
Genus: Macroderma
Species:
M. gigas
Binomial name
Macroderma gigas
(Dobson, 1880)[2]
Ghost bat range
Synonyms

Megaderma gigas

The ghost bat (Macroderma gigas) is a species of bat found in northern Australia. It is the only Australian bat that preys on large vertebrates – birds, reptiles and other mammals – which they detect using acute sight and hearing, combined with echolocation, while waiting in ambush at a perch. The wing membrane and bare skin is pale in colour, their fur is light or dark grey over the back and paler at the front. The species has a prominent and simple nose-leaf, with large elongated ears that are joined at the lower half, sharp teeth for attacking prey and large dark eyes. The first description of the species was published in 1880, since when its recorded range has significantly contracted.

Taxonomy

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A species of Macroderma, one of several genera in the family Megadermatidae (false vampires). The family all have large eyes, a nose-leaf and tragus, long ears joined at the base, and are also found in southern Asia and central Africa. The description was published in 1880 by George Dobson, emerging from an examination of specimens held by the Göttingen Museum. The author compared his specimen to taxa named as species of Megaderma, identifying species Megaderma spasma (lesser false vampire bat) as the closest in resemblance.[2][3] A revision of bat genera by Gerrit Smith Miller Jr. reassigned the species to a new genus Macroderma, creating the current generic combination.[4] The name Macroderma gigas combines the Greek words macros (large) and derma (skin), due to the large size of their partially conjoined ears (Richards, 2012).[5] The epithet gigas (giant) denotes it as the largest species in the family (Hudson, 1986).[6] The species M. gigas is placed with the Megadermatidae. An arrangement separating a "Pilbara district" population as subspecies Macroderma gigas saturata is noted as synonymous with this species concept (MSW 3rd ed., 2005).[7][3]

The specimen had previously been described by Gerard Krefft in a communication to the Zoological Society of London, and had been forwarded to the Göttingen museum by Dr. Schuette.[2] The description and illustration were presented to the society in 1879, accompanied by the suggestion that it was an unnamed genus of Phyllostomatidae (New World leaf-nosed bats); a member of the society, Edward Richard Alston, proposed instead it was a species of Megaderma which were unknown in Australia.[8][2] The type locality is at the Wilson River near Mt Margaret in Queensland,[3] where the collector, also named Wilson, obtained the bat.[2] An earlier observation had been noted by Robert Austin in 1854 at Mount Kenneth while surveying the inland regions of Western Australia.[9]

Studies of brain structures indicate that Macroderma gigas is an intermediate and divergent species of the insectivorous microchiropterans and the carnivorous species from South America.[6]

Common names that refer to Macroderma gigas have included ghost bat, false vampire, false vampire bat, and Australian false vampire bat.[10][7] The name ghost bat derives from its distinct colouring, the predominant colour of its fur may be near white or pale grey.[6]

Description

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A larger species of microchiropterans (microbats) and the largest in Australia, the size is comparable to the megabat species (flying fox, fruitbat).[11] The fur colour is grey, ranging in tone from mid, sometimes dark, to very pale grey at the back and whitish at the ventral side and head.[12][13] The colour of populations is a geographic cline, becoming darker toward the coastal regions.[14] A ring at the eye is dark and colour of the wing membranes and other bare skin is pale and brownish. The interfemoral membrane extends the wing surface between the length of the legs.[13] The great length of the ear, from notch at head to tip, is 44 to 56 millimetres and they are fluted in form; the inner margins of the ears are fused for half their length.[12] The length of the prominent ears is twice that of the head, a seam at the inner margins stiffens these to keep them upright while in flight.[15]

Other measurements of the species are a 96 to 112 mm (3.8 to 4.4 in) range for the forearm length, 98 to 120 mm (3.9 to 4.7 in) for the combined length of the head and body, and a weight range of 75 to 145 g (2.6 to 5.1 oz).[12]

Illustration accompanying the first description, R. Mintern 1880

The eyes are comparatively large and well developed for nocturnal vision, a feature shared with the long-eared genera Nyctophilus. The nose-leaf is also large and prominent, and simple in form.[16] The nasal appendage is presumably similar in usage to the elaborate forms of the horse-shoe and leaf-nosed bat genera, manipulating, directing and receiving echolocation signals to detect prey. The lack of a tail, effectively absent, is a characteristic of the species. The membrane at the rear is, however, supported by a calcar at the ankle.[17] The teeth and short robust jaw allow the consumption of a wide variety of animals, either the flesh and bones of other vertebrate species or hard shells of larger invertebrates.[18] Ghost bats are known for their unique hunting behavior, which includes ambushing prey from perches and using their powerful jaws to capture and consume various vertebrates, including small mammals, birds, reptiles, and amphibians.[19] A pregnant bat possesses two sets of teats, one pair beneath the armpits provide milk from the mammary glands and another pair at the pubic area. The pubic teats do not have a lactational function, rather they act as purchase points for the new-born to be carried in flight by the mother.[20]

The voice is audible to humans, one sound resembles the avian species Petrochelidon ariel (fairy martin) and transliterated as 'dirrup dirrup'. This twittering call is given when the bat is excited or before leaving the roost to feed.[12][11] A chirp uttered by the species resembles crickets.[11] The species is generally quiet, but some vocalisation is known in captivity when a squealing sound accompanies a squabble over food. The twittering sound was reported in captivity as hunger, and young will continually emit a chirp when the mother is absent.[6]

Behaviour and diet

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Although Macroderma gigas is inactive during daylight hours, they do not hibernate. The colony size reduces in the austral winter, increasing when they gather to breed or females form maternity groups.[21]

They leave the roost several hours after sunset, alone, in pairs, or as small groups. Hunting occurs via a 'sit and wait' technique while suspended from a tree or as low surveys over vegetation.[11][6] The large ears allow the bat to hear prey moving on the ground. Field observations at Pine Creek using nightscope equipment reported seeing M. gigas suspended from a tree and dropping to catch large locusts detected moving through grass at ten to twenty metres distance.[22] They are also able to detect the echolocation signals of the microbats on which they prey.[23] The bat has good vision for a microchiropteran, and echolocation is also utilised to directly locate approaching prey.[15] They are able to visually locate birds roosting in trees, and budgerigars (Melopsittacus undulatus) are detected by their silhouettes against the evening light.[24] The budgie is a favoured food of the bat, which they detect by the flock's chatter while retiring for the night, and these are taken to a perch to be consumed head first, with the feet and wing parts eventually being discarded.[25]

Prey may be taken at or to the ground, where it is enveloped with the wings and killed with bites to the neck. The sharp teeth and strong jaws are able to subdue animals as large as the bar-shouldered dove, species Geopelia humeralis, that may weigh as much as 150 grams, although most prey is smaller. Bird and mammal remains are most frequently recorded in their scats.[25] Once located, an animal is held down via the thumb claws and killed by a single bite to the neck.[6] The prey is killed at the ground or in flight, and taken to a perch to be consumed, at an overhanging rock or smaller cave for this purpose.[12]

The family Megadermatidae is carnivorous, feeding on vertebrate species including arthropod, mammalian, amphibian and reptilian prey.[7][12] Large insects, small mice, other bats, other small mammals, small birds, frogs, Pygopodidae (legless lizards), geckos and snakes and also taken.[6][12][7][26] Macroderma gigas is formally referred to as a specialised carnivore, but they have been known to feed on insects if prey is scarce. Vertebrate prey is eaten much more frequently and is usually consumed at the site of capture.[6] Other species of microbats are taken in flight, including species of Taphozous (sheathtails), Saccolaimus (bentwings), horseshoe bats and the little cave eptesicus.[7][27] The microbat species consumed by M. gigas feed at a variety of habitat and altitudes, and includes those known to cohabit with this species at cave roosts.[27]

A study of the avian prey of the bat revealed that over fifty species of birds are targeted, in a range of sizes but a preference for those weighing less than 35 grams. Birds that roost in flocks make up a large part of the diet, and a quarter of the species are non-passerines. One nocturnal species of bird is recorded at their middens, the Australian owlet-nightjar Aegotheles cristatus. The examination of the remains of their middens has given support to interpretation of fossil depositions, that have similar assemblages of discarded remains, at the Riversleigh formations where this and other species of Macroderma are exceptionally well represented.[28]

Field workers report that the species is remarkably passive when handled,[14] whilst other workers have recorded and confirmed reports of Macroderma gigas preying on rodents caught in their pitfall traps.[29]

Distribution and habitat

[edit]
anterior view of ghost bat under sedation

The ghost bat is endemic to Australia. Three population centres are identified, the Northern Pilbara and Kimberley in Western Australia, the Top End of the continent and in Queensland.[30] The distribution of colonies is non-contiguous, and they usually occur in small isolated pockets within each region.[12] Analysis of fossil remains shows that distribution patterns within Australia changed, in waves of both expansion and contraction, and the probable cause was ecological changes resulting from the increasing aridity of the continent's climate.[6] Remains of the species have been found with other mammals at the Devils Lair archaeological site in Southwest Australia, including other predators such as Thylacinus cynocephalus and Sarcophilus harrisii that inhabited the region after the first peoples had arrived.[31] Little is known of the genetics of the ghost bat, although the colonies shows a high degree of genetic distinctiveness at a local and regional level.[1]

The southernmost record is Austin's 1854 note at Mt Kenneth.[6] A limestone cave site favoured by M. gigas is in the region of the Mitchell and Palmer rivers at Cape York.[21] They are occur around Shoalwater Bay at the east coast.[21] The species is well represented at Litchfield National Park, which provides important caves and habitat for a number of bat species in the northern regions near Darwin.[32] The largest recorded breeding colony of M. gigas is at a gold mine named Kohinoor at the Top End.[33] The mine was dug in the late nineteenth century.[34] Another well known breeding site is found at Nourlangie Rock in Kakadu National Park, a region that is protected by law.[35] It is also recorded in national parks at Mount Etna Caves NP and at Tunnel Creek where they cohabit with other bat species.[36][11] Small colonies have been recorded along the Victoria River and at Camooweal Caves NP.[11] The range extends in association with rocky cliffs, gorges, or outcrops along watercourses in the Kimberley region of northwest Australia.[36]

Built environments may be used as feeding grounds,[6] but the ghost bat selects daytime roosts in caves, sheltered rock crevices, boulder piles or disused mines; occupation of abandoned buildings is only occasionally reported.[37][11] A preference is given to sites with a complex of shafts or cavities and several openings to the outside.[12] Macroderma gigas favours these caves with multiple entrance ways as they are large enough to accommodate the greater wingspan of the species and allow an alternative exit when sensing a threat.[38] They require several suitable sites for rest, feeding and reproduction, and change locations seasonally.[21] The species is especially sensitive to disturbance by humans, and this contributes to the selection or abandonment of a roost site.[12]

The bat and the caves they occupied were well known to peoples of Australia, often informing field workers of their locations in central Australia; some sites were part of 'men's business' that imparted a story of the being to young initiates.[9]

Macroderma gigas is present in the fossil record of Australia and found at the Riversleigh World Heritage Area. The species was sympatric with others of the genus at Riversleigh. such as Macroderma malugara, and is the modern representative of a lineage that extends to at least the early Miocene epoch.[39]

Range decline

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Captives at Alice Springs Desert Park, located in the bats earlier range

The ghost bat was once widely distributed throughout Australia, and became restricted to a sparser population across northern regions.[35] The species was recorded three more times in the twenty years that followed its discovery, two at Alice Springs and one in the Pilbara.[9] Attempts to survey the distribution range began in 1961, when its earlier status as a relict and rare species was revised to indicate it was more widespread and disappearing in regions where it was known within living memory;[9] Hedley Finlayson interviewed Pitjanjarra elders (Anangu people) who knew of the species in the Musgrave, Mann and Tomkinson Ranges where it had not been seen for forty years.[40] The species had been observed across the central regions of Australia, and the desiccated remains have been found on cave floors in the Flinders Ranges. The skeletons have also been recorded in caves of the coast in the southwest of Australia. The range is now limited to regions near the coast and north of the Tropic of Capricorn.[41]

Researchers have noted the lack evidence for the species in former range, and the contraction to the north both before and after European settlement has been investigated. There are isolated congregations of bats in specified maternity sites in which the alleles expressed by the females are distinguishable; this implies that the separation of such populations extends through evolutionary time. This scattering into small sets of populations greatly raises the threat of extinction to the species.[42]

It is estimated that several thousand ghost bats remain in existence today.[6] Declines in population are expected to be reversed in part because of increased survival rates, not because of immigration from other isolated areas.[30] There are very few national parks that strive to protect the species at this time.[6] The decline has been correlated to the increasing range of the amphibian species Rhinella marina (Bufo marinus), known locally as the cane toad. Investigations of recorded sites found the bat absent when the toad reached their local habitat, combined with the evidence of occasional consumption and—in one example—found in the throat of a deceased bat, the advance of the cane toad is strongly implicated as the cause of their rapid decline.[43]

Reproduction

[edit]

During the breeding season, late October to early November, female bats congregate in groups and give birth to a single young.[6] The generation length is estimated at four years.[1] According to a study conducted on range of ghost bats in Australia, "female bats gave birth to a single young in late spring, but only 40% of females bred in their second year, increasing to 93% for females greater than 2 years old".[citation needed]

Maternity colonies are founded in large and open caves and occupied until the young are reared.[21] The teats are evident in females during the maternity season. The possession of anterior teats allows the new born to cling to the mother until the milk teeth are shed.[44] The young are born in the austral spring, are able to fly after seven weeks, and become fully weaned at sixteen weeks. As is the norm for microbats, only one young is produced by the mother.[14] The males play no part in the rearing of young.[44] The juvenile hunts with the mother until reaching an independent stage of its maturity.[7]

Ecology

[edit]

The associated species include the black flying fox Pteropus alecto, recorded at Tunnel Creek in the Kimberley.[45] A new species of parasite, the tick Argas macrodermae, was discovered on specimens of M. gigas, but as a microchiropteran is remarkably free of external parasitic organisms. The only record as host to an endoparasite is the filarial nematode species Josefilaria mackerrasae, described from specimens found on M. gigas in 1979.[46][6]

Macroderma gigas has few predators, and most competition of their nocturnal hunts is from medium-sized owls (Strigidae).[30] They will join other predators at a cave mouth where other bat species will exit, this example of multiple species feasting together with other carnivores is intensified in the season when young bats are emerging from their creche. These congregations include introduced species, cane toad Rhinella marina, feral cats and foxes, and natives such as pythons, birds of prey, quolls and large frogs of genus Litoria.[47]

The bat will often take prey to a feeding roost, where a midden is formed from the discarded remains.[11] The range of a species of skink, found in the Northern Territory, was extended to Queensland by a record at a feeding roost of M. gigas.[25]

Captive under artificial light Perth Zoo

The species is vulnerable to several anthropogenic hazards, one is barbed wire fencing that accounts for many deaths when they are snagged through the easily torn wing membrane while in flight. The damage caused by the barbed wire strands, often left littering their environment, is greatly increased as the individual become entangled as it attempts to dislodge itself.[48] A study in the Pilbara region identified this as an especial concern, with indications that barbed wire was significantly impacting local populations when erected. The foraging height of M. gigas is around that of the dominant Triodia (spinifex) vegetation and the species is unable to visually detect the wire strand, and is not thought to use echolocation to forage in flight.[49] The thorny and tangled introduced plant lantana also presents a similar hazard to bats.[1] They are especially sensitive to disturbance in wintering roosts, and a single fleeting visit will see the site deserted for several weeks or altogether if human activity continues.[50] Most bat species are vulnerable to human disturbance, but attempts to view M. gigas at their roosts are especially discouraged due to the rapid decline in range and population.[11] New or reopened mining operations may have an impact on local colonies, although they may provide diurnal roosts when complete; they are vulnerable to dilapidation in former mines such as the collapse of ceilings.[14]

The conservation status of Macroderma gigas includes listings of state or federal authorities and non-governmental organisations. The Queensland and South Australian state registers note the species as endangered and in Western Australia it is classified as vulnerable to threatening factors. The federal classification is vulnerable under the EPBC act 1999.[51] Despite a well documented decline, the relevant criteria of legislation was not found to support a relisting of their status as endangered without analysis of genetic variation in the population. The relevant non statuary bodies, IUCN and The action plan for Australian mammals (2012), also list this species as vulnerable to extinction.[51][1] The population estimate at the IUCN Red List (2021) is between four and six thousand mature individuals in total. The state population of Queensland is less than one thousand, and the large colony at Mt Etna has gone into decline. The Kohinoor maternity colony at the Top End is stable but vulnerable to mine collapse. The western populations are more numerous in the Kimberley, three to four thousand, and the Pilbara group is estimated at less than six hundred.[1]

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References

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Revisions and contributorsEdit on WikipediaRead on Wikipedia
from Grokipedia
The ghost bat (Macroderma gigas), also known as the Australian false vampire bat, is Australia's largest and only carnivorous , a pale-furred species renowned for its ghostly appearance and predatory habits on vertebrates such as birds, reptiles, and small mammals. Native exclusively to , including regions of Western Australia, the Northern Territory, and , the ghost bat inhabits arid savannas, tropical rainforests, and coastal areas, where it roosts in caves, shafts, and deep rock fissures, often in small colonies of up to several hundred individuals. Measuring 10–13 cm in body length with a of 10.2–11.2 cm, a of 50–60 cm, and weighing 130–170 grams, it features light grey to sooty-grey fur, large forward-facing ears joined at the base, prominent dark eyes for enhanced vision, and translucent pinkish-white wing membranes that contribute to its spectral look. Nocturnal and highly secretive, ghost bats employ both echolocation and acute eyesight to hunt, typically perching to ambush prey on the ground before delivering a powerful bite to subdue it, then transporting larger victims to designated feeding sites for consumption. Their diet is diverse and opportunistic, encompassing large , frogs, , birds, and even other bats, with occasional predation on like cane toads. Reproduction occurs seasonally, with mating in July–August, a three-month , and birth of a single pup between September and November; young are weaned by March and reach independence soon after. As the sole living member of its genus Macroderma within the family , the ghost bat has experienced significant range contraction since European settlement, now listed as Vulnerable nationally in and Endangered in and due to threats including from and , disturbance of roosting sites by , and predation pressures from introduced predators. Conservation efforts focus on protecting key sites, monitoring populations through bioacoustics, and minimizing human impacts to support recovery of this ecologically significant predator.

Taxonomy and evolution

Taxonomy

The ghost bat (Macroderma gigas) belongs to the order Chiroptera and the family , within the suborder . It is the only extant species in the monotypic Macroderma, which is endemic to . The species was first described in 1880 by George Edward Dobson as Megaderma gigas, based on a specimen collected from Mount Margaret on the Wilson River in central Queensland, . In 1906, Gerrit Smith Miller Jr. erected the Macroderma and transferred the species to it, distinguishing it from the morphologically similar Old World Megaderma based on differences in finger bone proportions and overall cranial features. Common names for M. gigas include ghost bat and Australian false vampire bat. The designation "false vampire" stems from historical misconceptions that members of the , with their large size, prominent canines, and carnivorous habits, were blood-feeding like the true vampire bats (family Phyllostomidae), though they instead prey on vertebrates and using those enlarged canines to subdue live quarry. Phylogenetically, M. gigas is positioned within the as a basal Australian representative of carnivorous megadermatids, closely related to false vampires such as those in the genus Megaderma; mitochondrial genome analyses confirm it as the sister taxon to Megaderma lyra, with divergence estimated around the .

Fossil record

The fossil record of the ghost bat (Macroderma gigas) and its relatives in the genus Macroderma reveals a long evolutionary history in , with remains documented from Pleistocene deposits spanning northern to southern regions, suggesting a formerly more extensive distribution across the . Subfossil and Pleistocene specimens have been recovered from sites in southwestern , , and southeastern , including cave deposits at Cliefden, , and Yessabah Caves, where they date to the and indicate persistence in now-marginal habitats. These findings highlight a contraction in range since the Pleistocene, with the species absent from southern areas in modern records. The Macroderma encompasses several extinct species, providing insights into its prehistoric diversity. One such species, Macroderma malugara, is known from middle fossils at the Site in the Riversleigh World Heritage Area, northwestern , where dental and cranial remains exhibit traits transitional between earlier megadermatids and later forms. Other extinct congeners, including Macroderma koppa from deposits, further illustrate the genus's variation in size and morphology during the Tertiary. The Megadermatidae family, to which Macroderma belongs, originated in the Australia-New Guinea region, with the Australian fossil record documenting seven species from the Oligo-Miocene onward. Evolutionary adaptations for carnivory, such as robust dentition and enlarged canines suited for vertebrate prey, emerged prominently during the Miocene, as evidenced by trends in facial shortening and dental specialization in the Macroderma lineage across Riversleigh sites. This lineage shows evidence of independent gigantism in multiple branches, reflecting ecological diversification in ancient Australian ecosystems. The Macroderma divergence from other megadermatids is estimated around the Oligo-Miocene boundary, approximately 25–30 million years ago, based on the earliest Australian fossils and phylogenetic trends in the .

Physical description

Morphology

The ghost bat (Macroderma gigas) is Australia's largest , characterized by its substantial size relative to other Australian insectivorous and carnivorous . Adults typically weigh 130–170 g, with forearm lengths ranging from 96–113 mm and a reaching up to 60 cm. These measurements underscore its robust build, adapted for agile flight and prey capture, distinguishing it from smaller sympatric bat . The fur is sparse across the body, providing a semi-naked appearance, and varies regionally in coloration: pale to dark grey on the dorsal surface and whitish or pale grey on the ventral surface. This light pelage contributes to its ghostly pallor, especially in arid populations where it appears almost ashy-white overall. Prominent head features include large, dark eyes suited for low-light vision, a simple and protruding nose-leaf, and elongated ears that are joined at their base by a thin , often with a notched tragus. The body lacks an external tail, a distinctive trait among megadermatid bats, and possesses robust limbs ending in sharp claws for grasping prey. The features sharp, carnassial-like teeth specialized for tearing flesh from and prey. Wing membranes are pale, translucent, and extend from elongated fingers, forming long, narrow wings that enhance maneuverability. Sexual dimorphism is subtle, with males generally slightly larger than females in body size and mass.

Sensory adaptations

The ghost bat (Macroderma gigas) possesses large, well-developed eyes adapted for nocturnal vision, enabling effective prey detection in low-light conditions unlike many echolocating bats that rely primarily on . These eyes provide a approaching two cycles per degree, based on density, which supports visual guidance during flight and . While eye size is notable (detailed in morphology), this allows the bat to scan environments and identify targets before engaging echolocation. Echolocation in the ghost bat involves low-intensity, steep frequency-modulated pulses sweeping from approximately 60 kHz to 15 kHz, suited for close-range avoidance and precise prey localization rather than long-distance detection. These broad-band calls, with durations of about 0.7 milliseconds at rest and 1.2 milliseconds in flight, are often emitted through the nostrils and can be "whispered" intermittently to minimize alerting prey. This system complements rather than dominates navigation, as evidenced by studies showing intact flight performance through apertures even with eyes covered, though vision enhances braking control. Auditory adaptations feature large, elongated ears with a forked tragus, providing acoustic gain of 25–30 dB in the 5–8 kHz range for enhanced passive listening to prey-generated sounds such as rustling or vocalizations. This sensitivity allows detection of subtle environmental cues, including those from potential prey in roosts, and supports the bat's strategy by amplifying low-frequency echoes and airborne noises. The ghost bat exhibits a moderate olfactory sense, utilizing smell to detect prey scents within roosts or foraging sites, which stimulates activity and aids in environmental orientation. These sensory modalities integrate into a multimodal strategy, where vision identifies broad targets, passive hearing localizes sounds, and echolocation refines close-proximity details, enabling efficient and prey pursuit in complex nocturnal habitats. This combined approach distinguishes the ghost bat from more sonar-dependent species, optimizing its carnivorous lifestyle.

Habitat and distribution

Geographic range

The ghost bat (Macroderma gigas) is endemic to and currently occupies a fragmented distribution across the northern part of the continent. Its range includes the and Kimberley regions of Western Australia, the Top End of the (including areas like and the ), and northern from to . In , the species persists in only 4–5 highly disjunct populations, centered around key maternity roosts such as Mount Etna. These populations are genetically isolated, with western groups ( and Kimberley) separated from eastern ones ( and ) by distances exceeding 300 km, and no confirmed records in since the 1960s. Historically, the ghost bat's distribution extended farther south, encompassing arid and semi-arid zones across much of , including central deserts, , and , as evidenced by subfossil remains and early 20th-century records. The species' range has contracted northward over the and accelerated since European settlement, resulting in the of southern populations and a shift toward tropical and subtropical northern habitats. Post-2020 surveys estimate the total population at fewer than 10,000 individuals as of 2021, with regional breakdowns including fewer than 1,000 in , 2,500–3,500 in the , approximately 1,850 in the , and 3,000–4,000 in the Kimberley. A June 2025 thermal imaging survey recorded 463 individuals in 's largest known colony. Recent monitoring highlights continued fragmentation, with declines in some colonies attributed to habitat alterations and influences, though the overall distribution remains confined to these northern enclaves.

Habitat preferences

The ghost bat (Macroderma gigas) primarily roosts in caves, deep rock crevices, and abandoned mines, favoring humid, dark enclosures that offer stable microclimates and protection from predators. These sites typically include deep chambers with elevated spaces over 1.5 meters high, rough domed ceilings for gripping, and multiple access points to facilitate escape. Roosts are categorized by usage frequency, with permanent maternity sites in larger caves supporting colonies of up to several hundred individuals, while occasional or opportunistic roosts may consist of shallow overhangs or piles. For foraging, ghost bats prefer tropical savannas, dry woodlands, arid spinifex hillsides, shrublands, and riparian zones, often selecting areas near water bodies where prey is abundant. They forage up to 12–25 km from roosts, using vantage points in thin mature woodlands or tussock grasslands, but avoid open grasslands lacking cover. Proximity to productive plains and watercourses enhances prey availability, with average foraging areas spanning about 61 hectares. Microhabitat requirements emphasize stable environmental conditions, including temperatures of 25–31°C and levels above 70%, occasionally reaching 100% during wet seasons to support and . Seasonally, bats shift to larger caves for maternity roosts during breeding periods, which vary by region—July–August in the and October–November in the and —while using temporary day roosts in trees or buildings outside peak reproduction. In the , individuals may disperse to alternative sites based on prey and . Ghost bats exhibit high sensitivity to disturbance, frequently abandoning roosts after intrusion, vibrations exceeding 10 mm/s peak , or artificial lighting, which can lead to site desertion for months or years. This vulnerability underscores the need for undisturbed enclosures with multiple exits to minimize predation risks during such events.

Behavior

Foraging and diet

The ghost bat employs a perch-hunting ambush strategy, perching on elevated vantage points such as tree branches or rocks to scan for prey using both sight and echolocation before launching brief aerial attacks. It often gleans prey directly from the ground, foliage, or cave walls after detecting subtle sounds of movement, swooping feet-first to capture items mid-air or from surfaces. These sensory adaptations enable precise targeting in low-light conditions. The diet of the ghost bat is primarily composed of vertebrates, including small mammals (such as , dasyurids, and other bats), birds (e.g., budgerigars and finches), reptiles (e.g., geckos and skinks), and frogs, with serving as a secondary source, particularly large like beetles, locusts, and moths, which are hawked in flight or gleaned from . Prey selection is opportunistic, varying by region and season; for instance, in the region of , vertebrates dominate at approximately 96% (with mammals at 70% and birds at 24%), while contribute only 4%. Ghost bats target prey up to 50% of their own body weight (around 75 g for adults weighing 150 g), lifting smaller items (1-60 g) to temporary feeding perches and dismembering larger ones on the ground before consuming the flesh, while discarding indigestible parts like bones, fur, and feathers. occurs within 2-5 km of roosts, covering areas of about 60 ha nightly, with activity peaking 1-3 hours after sunset during nocturnal hunts that last 30-300 minutes per site. Daily energy intake averages 20-30 g of per individual, equivalent to one or day-old chick supplemented by , supporting their high metabolism without . In dry periods, the diet shifts toward a higher proportion of when prey becomes scarcer due to reduced availability.

Social structure

Ghost bats (Macroderma gigas) form colonies that typically range from 5 to 100 individuals, though aggregations can reach up to 600 in abandoned mines and historical sites. These colonies display fission-fusion dynamics, with individuals or small groups shifting between roosts in response to fluctuations in prey availability or environmental disturbances. Colony sizes tend to vary seasonally, often increasing during periods of higher resource abundance. The social structure within roosts is loose, without evidence of strict dominance hierarchies. Males defend small territories inside the roost, particularly during periods of heightened activity such as or juvenile flights. Communication among ghost bats relies on a repertoire of social vocalizations, including chirp-trills used for territorial defense and coordination (primarily by males), squabbles and rasps during agonistic encounters, grumbles for , with frequencies typically ranging from 1 to 15 kHz. Daily routines center on diurnal roosting in caves or mines, followed by 2–3 hours after sunset for foraging and other activities. Within colonies, individuals perform self-grooming behaviors such as body and face grooming, while allogrooming—often involving nuzzling or urogenital sniffing—occurs infrequently and is associated with vocalizations like grumbles. Ghost bats do not engage in long-distance migration but undertake limited local movements between roosts, typically up to 30 km, driven by seasonal changes or resource needs.

Reproduction

Breeding biology

Parturition in the ghost bat (Macroderma gigas) varies by latitude across its northern Australian range, with births typically occurring from mid-October to late November in and the region of , while earlier in July–August in the Top End of the . This timing often coincides with the onset of the , which provides increased prey availability to support reproductive demands. occurs during the , generally from April to August, with regional variation to align with the approximately 90–100 day period leading to these birth timings. is synchronized among females within colonies, contributing to a sharply defined and nearly synchronous birthing pattern across populations. The is polygynous, with males siring from multiple females during a single breeding season. Males attract females and repel rivals through vocal displays, including chirp-trills and squabbles that increase in frequency during the period, often produced from perches within roosts. Following , lasts approximately 90–100 days, after which females give birth to a single young. The ghost bat exhibits a low reproductive rate, producing 0.8–1.0 young per female annually due to the single litter size and annual breeding cycle. During this period, females form maternity colonies in large, stable caves or rock shelters, such as those at Mt. Etna in or Tolmer Falls in the , where they aggregate for protection and . A high degree of female drives this site fidelity, with females often returning to or remaining at their natal roosts, reinforcing genetic structure within populations.

Development of young

Ghost bat pups are born in a highly altricial state, lacking and with their eyes closed, typically weighing approximately g at birth. This initial vulnerability requires complete dependence on the mother for survival and in the maternity roosts where births occur. The period extends for 4–6 weeks, during which the mother's , rich in content, facilitates rapid growth and development of the pup's musculoskeletal system and energy reserves. Pups remain attached to the false teats in the mother's armpits during this phase, allowing her to carry them while . begins around 3–4 months, marking the transition to solid food as pups start accompanying mothers on hunts to learn skills. Flight development is a critical milestone, with pups achieving their first flights at approximately 7 weeks of age, though full proficiency and independence are not attained until 4–5 months. remains intensive during this period, with females transporting pups to safer ing sites if needed and providing from predators. Juvenile to adulthood is approximately 25–50%, influenced by factors such as disturbance, food availability, and birth timing, while dispersal from the natal typically occurs between 6 and 12 months as young bats establish their own territories.

Ecology and conservation

Ecological interactions

The ghost bat (Macroderma gigas) occupies an apex position as a carnivorous predator and within northern Australian ecosystems, controlling populations of small vertebrates such as birds, reptiles, frogs, and mammals, as well as large and occasionally other bats. Due to its relatively large size (average mass around 150 g), the ghost bat experiences rare predation from natural enemies, primarily larger owls that hunt at night, such as the (Ninox connivens), which are known to prey on bats. Young ghost bats in roosts may also fall prey to snakes or other roost-dwelling predators. The ghost bat faces competition for prey resources from other carnivorous or insectivorous bats, such as medium-sized in the genus Taphozous, and from that overlap in targeting small vertebrates and . Specific parasites of the ghost bat include the tick Argas (Carios) macrodermae, described from specimens collected on the species, and the filarial Josefilaria mackerrasae, a parasite found in Australian populations; overall, the species exhibits a low parasite load compared to many other microchiropterans. Symbiotic relationships are limited, but the ghost bat contributes indirectly to and through its predation on fruit- and nectar-eating prey , whose digestive remains may facilitate these processes.

Threats and conservation

The ghost bat (Macroderma gigas) faces multiple human-induced threats that have contributed to its population declines. , primarily from mining activities and vegetation clearing associated with cattle grazing, has led to the loss and isolation of critical roosting sites such as caves and mineshafts. Roost disturbance from human access, including noise, vibration, and helicopter overflights, further exacerbates this vulnerability, as ghost bats are highly sensitive to intrusions that disrupt maternity colonies. For instance, in February 2025, unauthorized cave access at Mount Etna in led to a maternity colony abandoning pups, resulting in deaths and highlighting the acute impact of recreational disturbance. The invasion of cane toads (Rhinella marina) since the 1930s has introduced toxic prey, causing direct mortality and localized population crashes, particularly in the Northern Territory. Additionally, collisions with fences pose a significant risk during flight, with multiple fatalities documented across . The species is classified as Vulnerable on the IUCN Red List, based on a 2021 assessment that highlights ongoing declines. Under Australia's Environment Protection and Biodiversity Conservation (EPBC) Act 1999, it holds Vulnerable status federally, while it is listed as Endangered in Queensland and South Australia due to severe regional threats. Population trends indicate a major range contraction since European settlement, with estimates indicating a contraction of more than 30% in occupied bioregions and an overall population of fewer than 10,000 individuals as of 2021, with continued declines, such as the Mount Etna colony reducing from approximately 450 in the 1960s to fewer than 50 individuals as of 2025. Recent genetic studies using non-invasive sampling have revealed significant landscape genetic structure, indicating low connectivity among populations and limited gene flow, which heightens extinction risk in isolated colonies. Conservation efforts focus on mitigating these threats through protected areas and targeted interventions. Key sites like provide essential refuges, safeguarding roosts from development. In 2024, a case study in 's Drovers Cave National Park assessed the feasibility of reintroduction, evaluating suitability and prey availability as a model for expanding southern range extents. Disturbance minimization protocols include establishing 100–250 meter buffer zones around roosts, restricting access during breeding seasons (October–December in and , July–September in the ), and promoting wildlife-friendly fencing to reduce collisions. Ongoing monitoring via acoustic surveys and genetic tracking is crucial for assessing trends and informing management, with programs like the Eastern Ghost Bat Monitoring emphasizing low-impact methods. Climate change poses an emerging threat by potentially altering prey availability through shifts in and distributions, underscoring the need for adaptive strategies to enhance connectivity and resilience.

References

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