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line:xlsx:hash://sha256/181a039844a33e66a35a457b7ece741051086608e425a040051b79581d606b97!/Sheet1!/L1093	application/vnd.openxmlformats-officedocument.spreadsheetml.sheet	N/A	N/A	N/A	Nyctophilus timoriensis [synonym of]	Nyctophilus timoriensis major	Nyctophilus timoriensis major	Nyctophilus major	Nyctophilus major	Nyctophilus major	Nyctophilus major	Nyctophilus major	Nyctophilus major	Nyctophilus major	Nyctophilus major	Nyctophilus major		[HMW] Nyctophilus major J. E. Gray, 1844 , Perth, Western Australia , Australia . As currently recognized, Nyctophilus includes seven species groups: major , goulds, microtis , bifax , microdon , geoffroyi , and howensis . Nyctophilus major is in the major species group along with N. corbeni and possibly N. daedalus . Nyctophilus and sister genus Pharotis have generally been included as a separate tribe in Vespertilioninae ( Nyctophilini ) or as a separate subfamily ( Nyctophilinae ), but genetic data from Nyctophilus have recently placed it sister to Chalinolobus in Vespertilionini . Nyctophilus major was previously included under N. timoriensis as a subspecies; however, the name timoriensis is considered a species inquirenda because of ambiguity of type locality, lack of definitive type specimen, and lack of an adequate enough description or illustration to identify the name to any currently recognized species. What was previously recognized as N. timoriensis has been broken into four distinct species: N. major , N. corbeni , N. sherrini , and N. shirleyae . Specimens of Nyctophilus from TimorIsland recently obtained by K. M. Helgen apparently bare resemblance to N. heran , but comparison of these specimens to other Nyctophilus has not been done, and the name fimoriensis will continue to go unused for now. Two subspecies recognized.; [batnames2022]  major species group. See Parnaby (2009) for the status of timoriensis and use of major. ; [MDD2022] split from timoriensis (now considered a nomen dubium/species inquirenda); [IUCN] This taxon was considered part of Nyctophilus timoriensis . It is now recognised as a separate species comprising two sub-species: Nyctophilus major tor , a sexually dimorphic form occupying the woodlands of temperate semi-arid and arid Western and South Australia, and N. m. major Gray, 1844 occupying the temperate forests of mesic south-western Australia (Parnaby 2009).; [batnames2023]  major species group. See Parnaby (2009) for the status of timoriensis and use of major. ; [MDD2023] split from timoriensis (now considered a nomen dubium/species inquirenda); [MDD2025_2.0] split from N. timoriensis; [batnames2025_1.7] major species group. Does not include timoriensis; see Parnaby and Helgen (2023). See Parnaby (2009) for the use of major.; [MDD2025_2.2] split from N. timoriensis										major, tor	timoriensis - unused	major, tor	tor - timoriensis	major, major, tor	This taxon was considered part of Nyctophilus timoriensis . It is now recognised as a separate species comprising two sub-species: Nyctophilus major tor , a sexually dimorphic form occupying the woodlands of temperate semi-arid and arid Western and South Australia, and N. m. major Gray, 1844 occupying the temperate forests of mesic south-western Australia (Parnaby 2009).	major, tor		major, tor 	major, tor 	major, tor		major J. E. Gray, 1841 [nomen nudum]|major J. E. Gray, 1844|tor Parnaby, 2009						N/A																																								_N. m. major_ Gray, 1844 (synonyms: _major_ Gray, 1841); _N. m. tor_ Parnaby, 2009																											4C3D87E8FFD06A68FA8593731B32BDF0	Handbook of the Mammals of the World – Volume 9 Bats, Barcelona: Lynx Edicions	978-84-16728-19-0	hbmw_9_Vespertilionidae_716.pdf.imf	hash://md5/b004ff90fffb6a44fffc96591e00bb32	801	zip:hash://sha256/ec5fd314a06aba1a7b0b72f23e54ac625ae272bd98f82f1d01f4c09627d9e8e0!/treatments-xml-main/data/4C/3D/87/4C3D87E8FFD06A68FA8593731B32BDF0.xml	Nyctophilus major	Vespertilionidae	Nyctophilus	major	J. E. Gray	1844	Nyctophile de Perth @fr | Gro Re Langohrfledermaus @de | Nictofila de Perth @es | Greater Long-eared Bat @en	Nyctophilus major J. E. Gray, 1844 , Perth, Western Australia , Australia . As currently recognized, Nyctophilus includes seven species groups: major , goulds, microtis , bifax , microdon , geoffroyi , and howensis . Nyctophilus major is in the major species group along with N. corbeni and possibly N. daedalus . Nyctophilus and sister genus Pharotis have generally been included as a separate tribe in Vespertilioninae ( Nyctophilini ) or as a separate subfamily ( Nyctophilinae ), but genetic data from Nyctophilus have recently placed it sister to Chalinolobus in Vespertilionini . Nyctophilus major was previously included under N. timoriensis as a subspecies; however, the name timoriensis is considered a species inquirenda because of ambiguity of type locality, lack of definitive type specimen, and lack of an adequate enough description or illustration to identify the name to any currently recognized species. What was previously recognized as N. timoriensis has been broken into four distinct species: N. major , N. corbeni , N. sherrini , and N. shirleyae . Specimens of Nyctophilus from TimorIsland recently obtained by K. M. Helgen apparently bare resemblance to N. heran , but comparison of these specimens to other Nyctophilus has not been done, and the name fimoriensis will continue to go unused for now. Two subspecies recognized.	N.m.major].E.Gray,1844—SWWesternAustralia. N. m. tor Parnaby, 2009 — WC (one record) & S Western Australia and S South Australia E to Eyre Peninsula.	Head-body 51-65 mm, tail 40-52 mm, ear 21-5-28-6 mm, forearm 37-6-48-4 mm; weight 11-17-5 g. Males are a little smaller than females. The Western Long-eared Bat has very large ears and unique simple noseleaf consisting of two ridges, one further on muzzle and another immediately above nostrils, with vertical groove in middle and furred trough between them. Dorsal pelage is dark grayish brown; venter is lighter grayish white. Rostrum, ears, and wing membranes are dark blackish brown. Rostrum is short and blunt, with ridge across muzzle over nostrils that is low, broad, and without vertical groove. Ears are very large and broad, with bluntly rounded tips, horizontal ribbing on inner surfaces, inward curved anterior edges, and smooth posterior edges (ears can fold back at top ofthick part of anterior edge); large and furred interauricular band crosses forehead between ears; tragus is small and bluntly rounded at tip, being convex on anterior margin. Glans penis has comparatively large urethral lappets, and distal part is simple and lacks any protrusions. Baculum is 4-2—4-6 mm long, with moderately thin shaft (but thick in terms of Nyctophilus ) that constricts right before tip in dorsal view; tip has very small notch in dorsal view, and base is strongly bifurcated; in lateral view, baculum is curved downward at base, but shaftis straight to narrowed tip. Skull is robust and narrower than in Corben’s Long-eared Bat (N. cor beni) but broader than in the Tasmanian Long-eared Bat (NV. sherrini ); rostrum is short, broad, and robust; braincase is narrow, zygomatic arches are less rounded compared with Corben’s Long-eared Bat, and palate is longer; sagittal and lambdoidal crests are moderately developed; and M? and lower molars are extremely reduced. Dental formula for all species of Nyctophilusis11/3,C1/1,P1/2,M 3/3 (x2) = On following pages: 80. Corben’s Long-eared Bat ( Nyctophilus corbeni ); 81. Pallid Long-eared Bat ( Nyctophilus daedalus ); 82. Gould's Long-eared Bat ( Nyctophilus gould); 84. New Caledonian Long-eared Bat ( Nyctophilus nebulosus ); 85. Papuan Long-eared Bat ( Nyctophilus microtis ); 86. Pygmy Long-eared Bat ( Nyctophilus walker ); 87. Eastern Long-eared Bat ( Nyctophilus bifax ); 88. Northern Long-eared Bat ( Nyctophilus arnhemensis ); 89. Mount Missim Long-eared Bat ( Nyctophilus shirleyae ); 90. Small-toothed Long-eared Bat ( Nyctophilus microdon ); 91. Lesser Long-eared Bat ( Nyctophilus geoffroyi ); 92. Sunda Long-eared Bat ( Nyctophilus heran ); 93. Lord Howe Long-eared Bat ( Nyctophilus howensis ).	Generally Banksia ( Proteaceae ) woodlands, Casuarina ( Casuarinaceae ) and Melaleuca ( Myrtaceae ) forests, and tall eucalypt forests with high annual rainfall, preferring habitats with well-developed shrub understories.	Western Long-eared Bats primarily forage by perch-hunting, and they use passive listening with their large ears to locate prey; they probably use echolocation in some cases. Crickets are common prey, but a variety of other insects are eaten. They are known to glean insects off the ground and also have been observed foraging on the ground at times. They are slow fliers (6-9 km/h while foraging), but they have higher wing loading than other species of Nyctophilus , implying higher flight speed.	Western Long-eared Bats breed once a year in March—May; captive individuals have copulated as late as June. Spermatogenesis begins in November, and peak testicular size is attained in March, declining until May when males have enlarged epididymides but not enlarged testes. Sperm storage in females occurs in cauda isthmus of the oviduct and endometrial glands near utero-tubal junction; ovulation and fertilization are delayed until late August or September. Twins are born from late October to November, and volant young are first noted in December. Lactating females can be captured until February when young are weaned.	Western Long-eared Bats are nocturnal. They spend the day roosting in hollows and fissures of tree trunks and limbs and leave around dusk to forage. They often roost in mature or dead Eucalyptus rudis and Melaleuca rhaphiophylla (both Myrtaceae ). They are able to enter torpor to conserve energy during harsh conditions and during the day as needed. Their body temperature is normally 35°C, but it can drop to within 1-5°C of ambient temperature. Torpor provides metabolic savings of ¢.95% under ambient temperatures of5-15°C. They reportedly enter torpor at ambient temperatures of5-23°C and can spontaneously arouse at any time. They can maintain torpor for ¢.60 days straight if they rely solely on fat reserves. Call shape is very steep FM sweep, with peak frequencies of 42-47 kHz (mean 44-4 kHz) that cannot be easily identified from other long-eared bats.	Western Long-eared Bats roost alone or in pairs, and they switch roosts often, only staying at a roost for 1-2 days. They only move a short distance between each roost, and roosts are located relatively close to foraging areas, resulting in travel of ¢. 1200 m to feed.	Not assessed on The IUCN Red List. The Western Long-eared Bat has a wide distribution and does not seem to have any major threats.	Bailey & Haythornthwaite (1998) | Bullen & McKenzie (2002a, 2002b) | Churchill (2008) | Hosken (1996, 1997a, 1997b) | Hosken, Bailey et al. (1994) | Hosken, Blackberry et al. (1998) | McKenzie (2008) | Parnaby (2009)	https://zenodo.org/record/6397936/files/figure.png	79. Western Long-eared Bat Nyctophilus major French: Nyctophile de Perth / German: GroRe Langohrfledermaus / Spanish: Nictofila de Perth Other common names: Greater Long-eared Bat Taxonomy. Nyctophilus major J. E. Gray, 1844 , Perth, Western Australia , Australia . As currently recognized, Nyctophilus includes seven species groups: major , goulds, microtis , bifax , microdon , geoffroyi , and howensis . Nyctophilus major is in the major species group along with N. corbeni and possibly N. daedalus . Nyctophilus and sister genus Pharotis have generally been included as a separate tribe in Vespertilioninae ( Nyctophilini ) or as a separate subfamily ( Nyctophilinae ), but genetic data from Nyctophilus have recently placed it sister to Chalinolobus in Vespertilionini . Nyctophilus major was previously included under N. timoriensis as a subspecies; however, the name timoriensis is considered a species inquirenda because of ambiguity of type locality, lack of definitive type specimen, and lack of an adequate enough description or illustration to identify the name to any currently recognized species. What was previously recognized as N. timoriensis has been broken into four distinct species: N. major , N. corbeni , N. sherrini , and N. shirleyae . Specimens of Nyctophilus from TimorIsland recently obtained by K. M. Helgen apparently bare resemblance to N. heran , but comparison of these specimens to other Nyctophilus has not been done, and the name fimoriensis will continue to go unused for now. Two subspecies recognized. Subspecies and Distribution. N.m.major].E.Gray,1844—SWWesternAustralia. N. m. tor Parnaby, 2009 — WC (one record) & S Western Australia and S South Australia E to Eyre Peninsula. Descriptive notes. Head-body 51-65 mm, tail 40-52 mm, ear 21-5-28-6 mm, forearm 37-6-48-4 mm; weight 11-17-5 g. Males are a little smaller than females. The Western Long-eared Bat has very large ears and unique simple noseleaf consisting of two ridges, one further on muzzle and another immediately above nostrils, with vertical groove in middle and furred trough between them. Dorsal pelage is dark grayish brown; venter is lighter grayish white. Rostrum, ears, and wing membranes are dark blackish brown. Rostrum is short and blunt, with ridge across muzzle over nostrils that is low, broad, and without vertical groove. Ears are very large and broad, with bluntly rounded tips, horizontal ribbing on inner surfaces, inward curved anterior edges, and smooth posterior edges (ears can fold back at top ofthick part of anterior edge); large and furred interauricular band crosses forehead between ears; tragus is small and bluntly rounded at tip, being convex on anterior margin. Glans penis has comparatively large urethral lappets, and distal part is simple and lacks any protrusions. Baculum is 4-2—4-6 mm long, with moderately thin shaft (but thick in terms of Nyctophilus ) that constricts right before tip in dorsal view; tip has very small notch in dorsal view, and base is strongly bifurcated; in lateral view, baculum is curved downward at base, but shaftis straight to narrowed tip. Skull is robust and narrower than in Corben’s Long-eared Bat (N. cor beni) but broader than in the Tasmanian Long-eared Bat (NV. sherrini ); rostrum is short, broad, and robust; braincase is narrow, zygomatic arches are less rounded compared with Corben’s Long-eared Bat, and palate is longer; sagittal and lambdoidal crests are moderately developed; and M? and lower molars are extremely reduced. Dental formula for all species of Nyctophilusis11/3,C1/1,P1/2,M 3/3 (x2) = On following pages: 80. Corben’s Long-eared Bat ( Nyctophilus corbeni ); 81. Pallid Long-eared Bat ( Nyctophilus daedalus ); 82. Gould's Long-eared Bat ( Nyctophilus gould); 84. New Caledonian Long-eared Bat ( Nyctophilus nebulosus ); 85. Papuan Long-eared Bat ( Nyctophilus microtis ); 86. Pygmy Long-eared Bat ( Nyctophilus walker ); 87. Eastern Long-eared Bat ( Nyctophilus bifax ); 88. Northern Long-eared Bat ( Nyctophilus arnhemensis ); 89. Mount Missim Long-eared Bat ( Nyctophilus shirleyae ); 90. Small-toothed Long-eared Bat ( Nyctophilus microdon ); 91. Lesser Long-eared Bat ( Nyctophilus geoffroyi ); 92. Sunda Long-eared Bat ( Nyctophilus heran ); 93. Lord Howe Long-eared Bat ( Nyctophilus howensis ). Habitat. Generally Banksia ( Proteaceae ) woodlands, Casuarina ( Casuarinaceae ) and Melaleuca ( Myrtaceae ) forests, and tall eucalypt forests with high annual rainfall, preferring habitats with well-developed shrub understories. Food and Feeding. Western Long-eared Bats primarily forage by perch-hunting, and they use passive listening with their large ears to locate prey; they probably use echolocation in some cases. Crickets are common prey, but a variety of other insects are eaten. They are known to glean insects off the ground and also have been observed foraging on the ground at times. They are slow fliers (6-9 km/h while foraging), but they have higher wing loading than other species of Nyctophilus , implying higher flight speed. Breeding. Western Long-eared Bats breed once a year in March—May; captive individuals have copulated as late as June. Spermatogenesis begins in November, and peak testicular size is attained in March, declining until May when males have enlarged epididymides but not enlarged testes. Sperm storage in females occurs in cauda isthmus of the oviduct and endometrial glands near utero-tubal junction; ovulation and fertilization are delayed until late August or September. Twins are born from late October to November, and volant young are first noted in December. Lactating females can be captured until February when young are weaned. Activity patterns. Western Long-eared Bats are nocturnal. They spend the day roosting in hollows and fissures of tree trunks and limbs and leave around dusk to forage. They often roost in mature or dead Eucalyptus rudis and Melaleuca rhaphiophylla (both Myrtaceae ). They are able to enter torpor to conserve energy during harsh conditions and during the day as needed. Their body temperature is normally 35°C, but it can drop to within 1-5°C of ambient temperature. Torpor provides metabolic savings of ¢.95% under ambient temperatures of5-15°C. They reportedly enter torpor at ambient temperatures of5-23°C and can spontaneously arouse at any time. They can maintain torpor for ¢.60 days straight if they rely solely on fat reserves. Call shape is very steep FM sweep, with peak frequencies of 42-47 kHz (mean 44-4 kHz) that cannot be easily identified from other long-eared bats. Movements, Home range and Social organization. Western Long-eared Bats roost alone or in pairs, and they switch roosts often, only staying at a roost for 1-2 days. They only move a short distance between each roost, and roosts are located relatively close to foraging areas, resulting in travel of ¢. 1200 m to feed. Status and Conservation. Not assessed on The IUCN Red List. The Western Long-eared Bat has a wide distribution and does not seem to have any major threats. Bibliography. Bailey & Haythornthwaite (1998), Bullen & McKenzie (2002a, 2002b), Churchill (2008), Hosken (1996, 1997a, 1997b), Hosken, Bailey et al. (1994), Hosken, Blackberry et al. (1998), McKenzie (2008), Parnaby (2009).	Simmons, N.B. and A.L. Cirranello. 2022B. Bat Species of the World: A taxonomic and geographic database. Accessed on 10/11/2022.	Vespertilionidae	Nyctophilus major	Nyctophilus		major	Gray	1844	0	Zool. Voy. H.M.S. "Erebus" and "Terror,"	12b, plate 21, fig. 2	Greater Long-eared Bat	<b> tor </b> Parnaby, 2009; timoriensis Geoffroy, 1906 [ nomen dubium ].	Australia, Western Australia, Perth	S Australia	Not listed.	Least Concern	 major species group. See Parnaby (2009) for the status of timoriensis and use of major. 	Mammal Diversity Database. (2023). Mammal Diversity Database (Version 1.11) [Data set]. Zenodo. https://doi.org/10.5281/zenodo.7830771 released 15 April 2023	Nyctophilus major	23	Western Long-eared Bat	Greater Long-eared Bat	Theria	Placentalia	Boreoeutheria	Laurasiatheria	CHIROPTERA	VESPERTILIONIFORMES	NA	NA	VESPERTILIONOIDEA	VESPERTILIONIDAE	VESPERTILIONINAE	VESPERTILIONINI	Nyctophilus	NA	major	J. E. Gray	1844	0	Nyctophilus_major	Gray, J. E. (1844). The zoology of the voyage of the H.M.S. Erebus & Terror, under the command of Captain Sir James Clark Ross, during the years 1839 to 1843. By authority of the Lords Commissioners of the Admiralty. Vol. 1. Mammalia, Birds. E. W. Janson, London, 12b.	https://www.biodiversitylibrary.org/item/31178#page/34/mode/1up	BM 1844.7.9.20		Perth, Western Australia, Australia.			major J. E. Gray, 1844|major J. E. Gray, 1841 [nomen nudum]|tor Parnaby, 2009	split from timoriensis (now considered a nomen dubium/species inquirenda)	Parnaby, H. E. (2009). A taxonomic review of Australian Greater Long-eared Bats previously known as Nyctophilus timoriensis (Chiroptera: Vespertilionidae) and some associated taxa. Australian Zoologist, 35(1), 39-81.	Australia	Oceania	Australasia/Oceania	LC	0	0	0	Nyctophilus_major	0	unmatched	NA	1	IUCN. 2022. The IUCN Red List of Threatened Species. Version 2022-1. https://www.iucnredlist.org. Accessed on [28 September, 2022].	90000000	Nyctophilus major	ANIMALIA	CHORDATA	MAMMALIA	CHIROPTERA	VESPERTILIONIDAE	Nyctophilus	major	Gray, 1844	This taxon was considered part of Nyctophilus timoriensis . It is now recognised as a separate species comprising two sub-species: Nyctophilus major tor , a sexually dimorphic form occupying the woodlands of temperate semi-arid and arid Western and South Australia, and N. m. major Gray, 1844 occupying the temperate forests of mesic south-western Australia (Parnaby 2009).	90000000	Nyctophilus major	Least Concern		2020	2019-08-15 00:00:00 UTC	3.1	English	<span class="datalabel1">Nyctophilus major <span class="datalabel1"> is assessed as Least Concern even though it is dependent on mature, long-unburnt forests and woodlands that, for the last century, have been extensively cleared for farming and timber, and thinned by logging, salinity, stock-grazing and/or extensive bushfires. It may be declining, but there is no data indicating a rate &gt;10% in 16.8 years (3 generations; GL = 5.6 years based on similar species; Pacifici et al. 2013).</span>	<p><span class="datalabel1">Nyctophilus major is found in areas of eucalypt forest and woodland (Eucalyptus diversicolor E. marginata, E. gomphocephala, Melaleuca raphiophylla and Corymbia calophylla forests. Eucalyptus salmonophloia, E. salubris, E. oleosa, E. ovularis, Allocasuarina heugeliana and Acacia accuminata woodlands) with a prominent shrub stratum, especially near granite outcrops and old dams. In these habitats it roosts in tree crevices, foliage or under loose bark (Hoskins 1996), and hunts in cluttered air spaces at shrub height and around the sides of understory thickets using slow, fluttering flight and gentle turns as it gleans surfaces for insects and spiders (Woinarski et al. 2014). It also ambushes passing airborne insects from a perch. It is known to enter torpor to conserve energy and water loss (Hoskins 1997). Young are born from spring to early summer; lactating females have been found in February. Females are 15% larger than males in arid parts of the species range, which separates their foraging niches.</p> <span class="datalabel1">At western end of the species range, Hoskins (1996) found roosting was solitary, that individuals moved between roost sites every few days, and that distances between capture sites and roosts were less than 1200 metres.</span>	Major threats include a severe degradation and loss of mature, long-unburnt forests and woodlands that, for the last century, have been extensively cleared for farming and timber, and thinned by logging, salinity, stock-grazing and/or extensive bushfires.	The species is inferred to have a population decline based on a declining habitat quality and loss. There are no data indicating a rate &gt;10% in 16.2 years (3 generations; GL = 5.6 years based on GL of similar species in Pacifici et al. 2013).	Decreasing	<span class="datalabel1">The species has an extensive distribution through the western temperate zone of Australia, specifically the Warren, southern Swan Coastal Plain, Jarrah Forest, southern Avon, Mallee, Coolgardie and Hampton bioregions of Western Australia, and the Eyre and southern Gawler bioregions of South Australia.	There is no known value in trading or commercial use of this species.	Terrestrial	This species is not known to occur in protected areas. Research is needed to assess the species population status and trends, ecology, and threats.	Australasian		FALSE	FALSE	Global	Simmons, N. B., & Cirranello, A. L. (2023). Batnames.org Species List Version 1.4 (1.4). Zenodo. https://doi.org/10.5281/zenodo.8136157 	Vespertilionidae	Nyctophilus		major	Gray	1844	0	Zool. Voy. H.M.S. "Erebus" and "Terror,"	12b, plate 21, fig. 2	Greater Long-eared Bat	<b> tor </b> Parnaby, 2009; timoriensis Geoffroy, 1906 [ nomen dubium ].	Australia, Western Australia, Perth	S Australia	Not listed.	Least Concern	 major species group. See Parnaby (2009) for the status of timoriensis and use of major. 	Nyctophilus major	1005761	23	Western Long-eared Bat	Greater Long-eared Bat	Theria	Placentalia	Boreoeutheria	Laurasiatheria	CHIROPTERA	VESPERTILIONIFORMES	NA	NA	VESPERTILIONOIDEA	Vespertilionidae	VESPERTILIONINAE	VESPERTILIONINI	Nyctophilus	NA	major	J. E. Gray	1844	0	Nyctophilus_major	Gray, J. E. (1844). The zoology of the voyage of the H.M.S. Erebus & Terror, under the command of Captain Sir James Clark Ross, during the years 1839 to 1843. By authority of the Lords Commissioners of the Admiralty. Vol. 1. Mammalia, Birds. E. W. Janson, London, 12b.	https://www.biodiversitylibrary.org/item/31178#page/34/mode/1up	BM 1844.7.9.20		Perth, Western Australia, Australia.			major J. E. Gray, 1844|major J. E. Gray, 1841 [nomen nudum]|tor Parnaby, 2009	split from timoriensis (now considered a nomen dubium/species inquirenda)	Parnaby, H. E. (2009). A taxonomic review of Australian Greater Long-eared Bats previously known as Nyctophilus timoriensis (Chiroptera: Vespertilionidae) and some associated taxa. Australian Zoologist, 35(1), 39-81.				Australia	Oceania	Australasia/Oceania	LC	0	0	0	Nyctophilus_major	0	unmatched	NA	1	Burgin, C. J., Zijlstra, J. S., Becker, M. A., Handika, H., Alston, J. M., Widness, J., Liphardt, S., Huckaby, D. G., and Upham, N. S. (2025). How many mammal species are there now? Updates and trends in taxonomic, nomenclatural, and geographic knowledge. Journal of Mammalogy in revision: TBD. https://doi.org/10.1101/2025.02.27.640393	Nyctophilus_major	1005761	23	Western Long-eared Bat	Greater Long-eared Bat	Theria	Placentalia	Boreoeutheria	Laurasiatheria	Chiroptera	Yangochiroptera	NA	NA	Vespertilionoidea	Vespertilionidae	Vespertilioninae	Vespertilionini	Nyctophilus	NA	major	J. E. Gray	0	Nyctophilus major	Gray, J.E. 1844-12-02. Part IV. Pp. 5â€“8 in Richardson, J. and Gray, J.E. 1844-1875. The Zoology of the Voyage of H.M.S. Erebus & Terror, under the command of Captain Sir James Clark Ross, R.N., F.R.S., during the years 1839 to 1843. Vol. I. Mammalia, Birds. E. W. Janson, London, not continuously paginated pp.	https://www.biodiversitylibrary.org/page/6957562	BMNH:Mamm:1844.7.9.20	holotype	https://data.nhm.ac.uk/object/b008bd0b-86fc-4788-baf9-b1f5084bdcfd	Perth, Western Australia, Australia.			split from N. timoriensis	Parnaby, H. E. (2009). A taxonomic review of Australian Greater Long-eared Bats previously known as Nyctophilus timoriensis (Chiroptera: Vespertilionidae) and some associated taxa. Australian Zoologist, 35(1), 39-81.				Australia	Oceania (Continent)	Australasia	LC	0	0	0	Nyctophilus_major	0	unmatched	NA	1	Simmons, N. B., & Cirranello, A. L. (2025). Batnames.org Species List Version 1.7 (1.7). Zenodo. https://doi.org/10.5281/zenodo.14796586	Vespertilionidae	Nyctophilus		major	Gray	1844	0	Zool. Voy. H.M.S. "Erebus" and "Terror,"	12b, plate 21, fig. 2	Greater Long-eared Bat	tor Parnaby, 2009; timoriensis Geoffroy, 1906 [nomen dubium].	Australia, Western Australia, Perth	S Australia	<a href='https://cites.org/eng/app/appendices.php' target='_blank'>Not Listed</a>	<a href='https://www.iucnredlist.org/species/85289614/85289618/' target='_blank'>Least Concern</a>	major species group. Does not include timoriensis; see Parnaby and Helgen (2023). See Parnaby (2009) for the use of major.		Mammal Diversity Database. (2025). Mammal Diversity Database (Version 2.2) [Data set]. Zenodo. https://doi.org/10.5281/zenodo.15007505	NA	Nyctophilus major; Nyctophilus major; Nyctophilus major; Nyctophilus major; Nyctophilus major; major; tor; timoriensis - unused; tor; tor - timoriensis; major; major; tor; Nyctophile de Perth; Gro Re Langohrfledermaus; Nictofila de Perth; Greater Long-eared Bat; Western Long-eared Bat; Greater Long-eared Bat; Greater Long-eared Bat; N. major
