http://www.w3.org/ns/prov#wasDerivedFrom	http://purl.org/dc/elements/1.1/format	name_CH1_1980	name_MSW1_1982	name_CH3_1991	name_MSW2_1993	name_Koopman_1994	name_MSW3_2005	name_HMW_2019	name_BatNames_2022	name_MDD_2022	name_IUCN_2022	name_BatNames_2023	name_MDD_2023	name_MDD_2025_2.0	name_batnames_2025_1.7	name_MDD_2025_2.2	column151	taxonomic_notes_concatenated	column171	synonyms_CH1	subspecies__MSW2	synonyms__MSW1	synonyms_CH3	synonyms_MSW2	subspecies_Koopman94_interpreted	subspecies_MSW3_interpreted	synonym_MSW3_interpreted	subspecies_HMW_interpreted	synonym_HMW_interpreted	subspecies_batnames_interpreted	synonym_batnames_interpreted	synonym_MDD_interpreted	synonym_IUCN_interpreted	subspecies_batnames2023_interpreted	synonym_batnames2023_interpreted	synonym_MDD2023_interpreted	synonym_MDD2025_interpreted	subspecies_batnames2025_interpreted	synonyms_batnames2025_interpreted	nominalNames	column391	docOrigin_CH1	commonName_CH1	distribution_CH1	docOrigin_MSW1	column451	typeLocality_MSW1	authority_MSW1	year_MSW1	citation_MSW1	distribution	comment_MSW1	docOrigin_CH3	commonName_CH3	distribution_CH3	docOrigin_MSW2	authority_MSW2	year_MSW2	citation_MSW2	comments_MSW2	distribution_MSW2	typeLocality_MSW2	docOrigin_Koopman94	authority_Koopman94	year_Koopman94	description_Koopman94	distribution_Koopman94	diversity_Koopman94	subspecies_Koopman94	page	rank	name	authority	year	parent	parent_rank	corrected_name	actual_species_count	claimed_species_count	dental_formula	description	diversity	full_subspecies_text	name_line	species_index	subspecies	synonym	text	docOrigin_MSW3	order_MSW3	family_MSW3	subfamily_MSW3	tribe_MSW3	name_MSW3	genus_MSW3	subgenus_MSW3	species_MSW3	authoritySpeciesAuthor_MSW3	(parentheses (1=author & date in parentheses)_MSW3	authoritySpeciesYear_MSW3	actualDate_MSW3	citation_MSW3	volume_MSW3	issue_MSW3	pages_MSW3	type_species_MSW3	commonName_MSW3	typeLocality_MSW3	distribution_MSW3	status_MSW3	synonym_MSW3	comments_MSW3	docId_HMW	docOrigin_HMW	docISBN_HMW	docName_HMW	docMasterId_HMW	docPageNumber_HMW	derivedFrom_HMW	name_HMW	family_HMW	genus_HMW	species_HMW	authoritySpeciesAuthor_HMW	authoritySpeciesYear	commonNames_HMW	taxonomy_HMW	subspeciesAndDistribution_HMW	descriptiveNotes_HMW	habitat_HMW	foodAndFeeding_HMW	breeding_HMW	activityPatterns_HMW	movementsHomeRangeAndSocialOrganization_HMW	statusAndConservation_HMW	bibliography_HMW	distributionImageURL_HMW	verbatimText_HMW	docOrigin_batnames	family_batnames	name_batnames	genus_batnames	subgenus_batnames	species_batnames	authoritySpeciesAuthor_batnames	date_batnames	parentheses_batnames (1=author & date in parentheses)	citation_batnames	docPageNumber_batnames	common Name_batnames	synonyms_batnames	type_locality_batnames	Distribution_batnames	CITES_batnames	IUCN_batnames	comments_batnames	docOrigin_MDD	name_MDD	phylosort_MDD	mainCommonName_MDD	otherCommonNames_MDD	subclass_MDD	infraclass_MDD	magnorder_MDD	superorder_MDD	order_MDD	suborder_MDD	infraorder_MDD	parvorder_MDD	superfamily_MDD	family_MDD	subfamily_MDD	tribe_MDD	genus_MDD	subgenus_MDD	specificEpithet_MDD	authoritySpeciesAuthor_MDD	authoritySpeciesYear_MDD	authorityParentheses_MDD	originalNameCombination_MDD	authoritySpeciesCitation_MDD	authoritySpeciesLink_MDD	holotypeVoucher_MDD	holotypeVoucherURIs_MDD	typeLocality_MDD	typeLocalityLatitude_MDD	typeLocalityLongitude_MDD	nominalNames_MDD	taxonomyNotes_MDD	taxonomyNotesCitation_MDD	countryDistribution_MDD	continentDistribution_MDD	biogeographicRealm_MDD	iucnStatus_MDD	extinct_MDD	domestic_MDD	flagged_MDD	CMW_sciName_MDD	diffSinceCMW_MDD	MSW3_matchtype_MDD	MSW3_sciName_MDD	diffSinceMSW3_MDD	docOrigin_IUCN	internalTaxonId_IUCN	NAME_IUCN	kingdomName_IUCN	phylumName_IUCN	className_IUCN	orderName_IUCN	familyName_IUCN	genusName_IUCN	speciesName_IUCN	authoritySpeciesAuthorYear_IUCN	taxonomicNotes_IUCN	assessmentId_IUCN	scientificName_IUCN	redlistCategory_IUCN	redlistCriteria_IUCN	yearPublished_IUCN	assessmentDate_IUCN	criteriaVersion_IUCN	language_IUCN	rationale_IUCN	habitat_IUCN	threats_IUCN	population_IUCN	populationTrend_IUCN	range_IUCN	useTrade_IUCN	systems_IUCN	conservationActions_IUCN	realm_IUCN	yearLastSeen_IUCN	possiblyExtinct_IUCN	possiblyExtinctInTheWild_IUCN	scopes_IUCN	docOrigin_batnames2023	FAMILY_batnames2023	GENUS_batnames2023	SUBGENUS_batnames2023	SPECIES_batnames2023	authoritySpeciesAuthor_batnames2023	authoritySpeciesYearbatnames2023	PARENTHESES_batnames2023 (1=AUTHOR & DATE IN PARENTHESES)	CITATION_batnames2023	PAGES_batnames2023	COMMON NAME_batnames2023	SYNONYMS_batnames2023	TYPE LOCALITY_batnames2023	DISTRIBUTION_batnames2023	CITES_batnames2023	IUCN_batnames2023	COMMENTS_batnames2023	name MDD2023	id_MDD2023	phylosort_MDD2023	mainCommonName_MDD2023	otherCommonNames_MDD2023	subclass_MDD2023	infraclass_MDD2023	magnorder_MDD2023	superorder_MDD2023	order_MDD2023	suborder_MDD2023	infraorder_MDD2023	parvorder_MDD2023	superfamily_MDD2023	Family_mdd2023	subfamily_MDD2023	tribe_MDD2023	genus_MDD2023	subgenus_MDD2023	specificEpithet_MDD2023	authoritySpeciesAuthor_MDD2023	authoritySpeciesYear_MDD2023	authorityParentheses_MDD2023	originalNameCombination_MDD2023	authoritySpeciesCitation_MDD2023	authoritySpeciesLink_MDD2023	holotypeVoucher_MDD2023	holotypeVoucherURIs_MDD2023	typeLocality_MDD2023	typeLocalityLatitude_MDD2023	typeLocalityLongitude_MDD2023	nominalNames_MDD2023	taxonomyNotes_MDD2023	taxonomyNotesCitation_MDD2023	distributionNotes_MDD2023	distributionNotesCitation_MDD2023	subregionDistribution_MDD2023	countryDistribution_MDD2023	continentDistribution_MDD2023	biogeographicRealm_MDD2023	iucnStatus_MDD2023	extinct_MDD2023	domestic_MDD2023	flagged_MDD2023	CMW_sciName_MDD2023	diffSinceCMW_MDD2023	MSW3_matchtype_MDD2023	MSW3_sciName_MDD2023	diffSinceMSW3_MDD2023	docOrigin_MDD2025	sciName	id	phylosort	mainCommonName	otherCommonNames	subclass	infraclass	magnorder	superorder	order	suborder	infraorder	parvorder	superfamily	family	subfamily	tribe	genus	subgenus	specificEpithet	authoritySpeciesAuthor	authorityParentheses	originalNameCombination	authoritySpeciesCitation	authoritySpeciesLink	typeVoucher	typeKind	typeVoucherURIs	typeLocality	typeLocalityLatitude	typeLocalityLongitude	taxonomyNotes	taxonomyNotesCitation	distributionNotes	distributionNotesCitation	subregionDistribution	countryDistribution	continentDistribution	biogeographicRealm	iucnStatus	extinct	domestic	flagged	CMW_sciName	diffSinceCMW	MSW3_matchtype	MSW3_sciName	diffSinceMSW3	docOrigin_batnames2025	Family	Genus	Subgenus	Species	Author	Date	Parentheses (1=author & date in parentheses)	Citation	Pages	Common Name	Synonyms	Type Locality	Distribution	CITES	IUCN	Comments	column3781	column3791	subtribe	CONCAT_ALTNAMES
line:xlsx:hash://sha256/181a039844a33e66a35a457b7ece741051086608e425a040051b79581d606b97!/Sheet1!/L387	application/vnd.openxmlformats-officedocument.spreadsheetml.sheet	Hipposideros diadema	Hipposideros diadema	Hipposideros diadema	Hipposideros diadema	Hipposideros diadema	Hipposideros diadema	Hipposideros diadema	Hipposideros diadema	Hipposideros diadema	Hipposideros diadema	Hipposideros diadema	Hipposideros diadema	Hipposideros diadema	Hipposideros diadema	Hipposideros diadema		[MSW3] diadema species group. Many subspecies are of dubious validity, and several island populations have not been assigned to subspecies. Reviewed in part by Laurie and Hill (1954) and Kitchener et al. (1992b). Does not include demissus and inornatus; see Kitchener et al. (1992b). Also see Flannery (1995a, b) and Bonaccorso (1998). May include ornatus, a name listed as a synonym of diadema by Koopman (1993) but which I have been unable to trace (although it may be a lapsus for inornatus).; [HMW] Rhinolophus diadema É. Geoffroy Saint-Hilaire, 1813 , “Timor [Island].” Hipposideros diadema is in the diadema species group. Many subspecies have been described (anderseni, ceramensis, custos, enganus, euotis, griseus, masoni, mirandus, natunensis, nicobarensis, nobilis, oceanitis, reginae, speculator, trobrius, vicarious), several of them of dubious validity; validity, diagnoses, and ranges of prospective subspecies require review.; [batnames2022]  diadema species group. Many subspecies are of dubious validity, and several island populations have not been assigned to subspecies. Reviewed in partby Laurie and Hill (1954) and Kitchener et al. (1992b). Does not include demissus and inornatus; see Kitchener et al. (1992b). Alsosee Flannery (1995a, b) and Bonaccorso (1998). Probably includes more than one species; see Esselstyn et al. 2012. May include ornatus, a name listed as a synonym of diadema by Koopman (1993) but which I have been unable to trace (although it may be a lapsus for inornatus). ; [IUCN] This species is recognized by Simmons and Cirranello (2020) and may have 15 subspecies (Bonaccorso 1998). Additional research is needed to clarify taxonomic relationships and distribution among the subspecies.; [batnames2023]  diadema species group. Many subspecies are of dubious validity, and several island populations have not been assigned to subspecies. Reviewed in partby Laurie and Hill (1954) and Kitchener et al. (1992b). Does not include demissus and inornatus; see Kitchener et al. (1992b). Alsosee Flannery (1995a, b) and Bonaccorso (1998). Probably includes more than one species; see Esselstyn et al. 2012. May include ornatus, a name listed as a synonym of diadema by Koopman (1993) but which I have been unable to trace (although it may be a lapsus for inornatus). ; [batnames2025_1.7] diademaspecies group. Many subspecies are of dubious validity, and several island populations have not been assigned to subspecies. Reviewed in partby Laurie and Hill (1954) and Kitchener et al. (1992b). Does not include demissus and inornatus; see Kitchener et al. (1992b). Alsosee Flannery (1995a, b) and Bonaccorso (1998). Probably includes more than one species; see Esselstyn et al. 2012. May includeornatus, a name listed as a synonym of diadema by Koopman (1993) but which I have been unable to trace (although it may be a lapsus for inornatus).						andersoni, ceramensis, custos, demissus, enganus, euotis, griseus, inornatus, malaitensis, masoni, mirandus, natunensis, nicobarensis, nobilis, oceanitis, ornatus, pullatus, reginae, speculator, trobrius, vicarius.	masoni, nicobarensis, natunensis, enganus, diadema, griseus, speculator, euotis, ceramicus, custos, pullatus, mirandus, trobrius, oceanitis, malaitensis, demissus, reginae, inornatus	diadema, ceramensis, custos, enganus, euotis, griseus, masoni, mirandus, natunensis, nicobarensis, nobilis, oceanitis, reginae, speculator, trobrius	griseus - anderseni, pullatus; nobilis - vicarius; oceanitis - malaitensis			diadema, ceramensis, custos, enganus, euotis, griseus, masoni, mirandus, natunensis, nicobarensis, nobilis, oceanitis, reginae, speculator, trobrius	griseus - anderseni, pullatus; nobilis - vicarius; oceanitis - malaitensis	diadema, nobilis, griseus, nicobarensis, masoni, bicarius , euotis, oceanitis, pullatus, enganus, mirandus, custos, speculator, anderseni , reginae, trobius, natunensis , ceramensis, malaitensis	This species is recognized by Simmons and Cirranello (2020) and may have 15 subspecies (Bonaccorso 1998). Additional research is needed to clarify taxonomic relationships and distribution among the subspecies.	diadema, ceramensis, custos, enganus, euotis, griseus, masoni, mirandus, natunensis, nicobarensis, nobilis, oceanitis, reginae, speculator, trobrius	griseus - anderseni, pullatus; nobilis - vicarius; oceanitis - malaitensis 	diadema, nobilis, griseus, nicobarensis, masoni, bicarius, euotis, oceanitis, pullatus, enganus, mirandus, custos, speculator, anderseni, reginae, trobius, natunensis, ceramensis, malaitensis	diadema, nobilis, griseus, nicobarensis, masoni, euotis, oceanitis, pullatus, vicarius, enganus, mirandus, custos, speculator, anderseni, reginae, trobrius, natunensis, ceramensis, malaitensis, andersoni	ceramensis, custos, diadema, enganus, euotis, griseus, masoni, mirandus, natunensis, nicobarensis, nobilis, oceanitis, reginae, speculator, trobrius	griseus - anderseni, pullatus; nobilis - vicarius; oceanitis - malaitensis	diadema (Ã‰. Geoffroy Saint-Hilaire, 1813)|nobilis (Horsfield, 1823)|griseus (Meyen, 1833)|nicobarensis (Dobson, 1871)|masoni (Dobson, 1872)|euotis Andersen, 1905|oceanitis Andersen, 1905|pullatus Andersen, 1905|vicarius Andersen, 1905|enganus Andersen, 1907|mirandus O. Thomas, 1914|custos Andersen, 1918|speculator Andersen, 1918|anderseni E. H. Taylor, 1934|reginae Troughton, 1937|trobrius Troughton, 1937|natunensis Chasen, 1940|ceramensis Laurie & J. Edwards Hill, 1954|malaitensis C. J. Phillips, 1967|andersoni M. A. Lawrence, 1993 [incorrect subsequent spelling]|ceramicus Koopman, 1994 [incorrect subsequent spelling]		Corbet, G.B. and Hill, J.E. 1980. A World List of Mammalian Species. British Museum (Natural History), London, 226 pp.	Diadem leaf-nosed bat	Burma – Java, Philippines, Borneo, New Guinea, Solomons, NE Queensland	Honacki, J.H., Kinman, K.E. and Koeppl, J.W. 1982. Mammal Species of the World: A Taxonomic and Geographic Reference. Allen Press, Lawrence, 694 pp.	Hipposideros diadema	Indonesia, Lesser Sunda Isis., Timor Isl.	E. Geoffroy	1813	Ann. Mus. Hist. Nat. Paris, 20:263.	Dis tribution: An extensive range from Burma and Vietnam south through the Malay peninsula and Sumatra and east to the Philippines, Solomons and tropical Australia.		Corbet, G.B. and Hill, J.E. 1991. A World List of Mammalian Species. Third edition. Oxford University Press, London, 243 pp. ISBN 0-19-854017-5	Diadem leaf-nosed bat	Burma – Java, Philippines, Borneo, New Guinea, Solomons, N Australia	Koopman, K.F. 1993. Order Chiroptera. Pp. 137–242 in Wilson, D.E. and Reeder, D.M. (eds.). Mammal Species of the World: A Taxonomic and Geographic Reference. Second edition. Smithsonian Institution Press, Washington, 1206 pp.	E. Geoffroy	1813	Ann. Mus. Hist. Nat. Paris, 20:263.		Burma and Vietnam through Thailand, W Malaysia and Indonesia to New Guinea, Bismarck Arch., Solomon Isis and NE and NC Australia; Philippines; Nicobar Isis.	Indonesia, Lesser Sunda Isis, Timor Isl.		GEOFFROY	1813	Frontal region concave with a shallow frontal depression. Interorbital region relatively narrow. Zygomatic arches markedly flared. Size relatively large (forearm length, 65-95 mm; con dylocanine length less than 31 mm; maxillary toothrow length less than 13.8 mm). Intermediate noseleaf with a prominent medial ridge.	Dis tribution: An extensive range from Burma and Vietnam south through the Malay peninsula and Sumatra and east to the Philippines, Solomons and tropical Australia.	Eighteen subspecies are currently recognized (though many are of dubious validity):	H. d. masoni (southeastern Asia, Sumatra, Borneo), H. d. nicobarensis (Nicobar islands), H. d. natunensis (North Natuna islands), H. d. enganus (Engano island, west of Su matra), H. d. diadema (Java, Lesser Sundas), H. d. griseus (Philippines), H. d. speculator (Celebes), H. d. euotis (Northern Moluccas), H. d. ceramicus (central Moluccas), H. d. custos (Keis), H. d. pullatus (New Guinea, Bismarcks), H. d. mirandus (Admirality islands), H. d. trobrius (Trob riand islands), H. d. oceanitis, H. d. malaitensis, H. d. demissus (all three in Solomons), H. d. reginae (northern Queensland, Australia), H. d. inornatus (northern North ern Territory, Australia).	66	species	H. diadema	GEOFFROY	1813	Hipposideros	genus	Hipposideros diadema				Frontal region concave with a shallow frontal depression. Interorbital region relatively narrow. Zygomatic arches markedly flared. Size relatively large (forearm length, 65-95 mm; con dylocanine length less than 31 mm; maxillary toothrow length less than 13.8 mm). Intermediate noseleaf with a prominent medial ridge.	Eighteen subspecies are currently recognized (though many are of dubious validity):		50. H. diadema (GEOFFROY 1813) [diadema group],	50	_H. d. ceramensis_ Laurie & Hill, 1954; _H. d. custos_ Andersen, 1918; _H. d. diadema_ (Geoffroy Saint-Hilaire, 1813); _H. d. enganus_ Andersen, 1907; _H. d. euotis_ Andersen, 1905; _H. d. griseus_ (Meyen, 1833) (synonyms: _anderseni_ Taylor, 1934, _pullatus_ Andersen, 1905); _H. d. masoni_ (Dobson, 1872); _H. d. mirandus_ Thomas, 1914; _H. d. natunensis_ Chasen, 1940; _H. d. nicobarensis_ (Dobson, 1871); _H. d. nobilis_ (Horsfield, 1823) (synonyms: _vicarius_ Andersen, 1905); _H. d. oceanitis_ Andersen, 1905 (synonyms: _malaitensis_ Phillips, 1967); _H. d. reginae_ Troughton, 1937; _H. d. speculator_ Andersen, 1918; _H. d. trobrius_ Troughton, 1937			Don E. Wilson & DeeAnn M. Reeder (editors). 2005. Mammal Species of the World. A Taxonomic and Geographic Reference (3rd ed), Johns Hopkins University Press, 2,142 pp. (Available from Johns Hopkins University Press, 1-800-537-5487 or (410) 516-6900, or at http://www.press.jhu.edu).	CHIROPTERA	Hipposideridae			Hipposideros diadema	Hipposideros		diadema	E. Geoffroy	y	1813		Ann. Mus. Natn. Hist. Nat. Paris	20		263		Diadem Leaf-nosed Bat	Indonesia, Lesser Sunda Isls, Timor Isl.	Burma and Vietnam through Thailand, Laos, W Malaysia and Indonesia (including Sumatra, Borneo, and Bali) to New Guinea, Bismarck Arch., Solomon Isls and NE Australia; Philippines; Nicobar Isls. Reports of this species from Cambodia cannot be confirmed (Kock, 2000a).	IUCN 2003 and IUCN/SSC Action Plan (2001) – Lower Risk (lc).	ceramensis Laurie and Hill, 1954; custos K. Andersen, 1918; enganus K. Andersen, 1907; euotis K. Andersen, 1905; griseus Meyen, 1883; anderseni Taylor, 1934; pullatus K. Andersen, 1905; masoni Dobson, 1872; mirandus Thomas, 1914; natunensis Chasen, 1940; nicobarensis Dobson, 1871; nobilis Horsfield, 1823; vicarius K. Andersen, 1905; oceanitis K. Andersen, 1905; malaitensis Phillips, 1967; reginae Troughton, 1937; speculator K. Andersen, 1918; trobrius Troughton, 1937.	diadema species group. Many subspecies are of dubious validity, and several island populations have not been assigned to subspecies. Reviewed in part by Laurie and Hill (1954) and Kitchener et al. (1992b). Does not include demissus and inornatus; see Kitchener et al. (1992b). Also see Flannery (1995a, b) and Bonaccorso (1998). May include ornatus, a name listed as a synonym of diadema by Koopman (1993) but which I have been unable to trace (although it may be a lapsus for inornatus).	03BD87A2C678A20AFF4EEE1BF55E48CD	Handbook of the Mammals of the World – Volume 9 Bats, Barcelona: Lynx Edicions	978-84-16728-19-0	hbmw_9_Hipposideridae_210.pdf.imf	hash://md5/ff84ffdac676a204fff8ff9affef4346	241	zip:hash://sha256/ec5fd314a06aba1a7b0b72f23e54ac625ae272bd98f82f1d01f4c09627d9e8e0!/treatments-xml-main/data/03/BD/87/03BD87A2C678A20AFF4EEE1BF55E48CD.xml	Hipposideros diadema	Hipposideridae	Hipposideros	diadema		1813	Phyllorhine à diadème @fr | Diadem-Rundblattnase @de | Hiposidérido de diadema @es | Diadem Roundleaf Bat @en	Rhinolophus diadema É. Geoffroy Saint-Hilaire, 1813 , “Timor [Island].” Hipposideros diadema is in the diadema species group. Many subspecies have been described (anderseni, ceramensis, custos, enganus, euotis, griseus, masoni, mirandus, natunensis, nicobarensis, nobilis, oceanitis, reginae, speculator, trobrius, vicarious), several of them of dubious validity; validity, diagnoses, and ranges of prospective subspecies require review.	Mainland SE Asia, Philippines , Indonesian Archipelago, New Guinea (including Bismarck Archipelago ), Solomon Is, and NE Australia ; also on N Nicobar Is .	Head—body 66-100 mm, tail 32—51 mm , ear 28—32 mm , hindfoot 16-21 mm, forearm 58—96 mm ; weight 22—57 g . Forearm length can be variable between populations, from as small as 58 mm ( Nicobar Islands ) to as large as 96 mm ( Thailand ). Pelage on upperparts is dark brown with distinctive white or yellowish white patches on shoulders and sides ofback; fur on underparts is grayish white. Noseleafis yellowish brown. Posterior noseleafis thick and tall. There are 3-4 lateral leaflets on each cheek. Skull is heavily built with large canine, inflated rostral swellings and well-developed sagittal crest P2 is small and extruded from tooth row so C1 and P4 are in contact, or almost. Chromosomal complement has 2n = 32 and FN = 60.	The Diadem Leaf-nosed Bat has been recorded in a wide range of habitats, from lowland primary forest at sea level to agricultural areas and disturbed forests up to 1210 m .	The Diadem Leaf-nosed Bat forages in forest understory, in gaps, and over streams in forest. It feeds on insects (Coleoptera, Lepidoptera , and various orthopteroids were the most common in fecal pellets) and occasionally on birds. It is known to feed by hanging from a perch and waiting for prey to pass by, then flying to snatch it and returning right away to the perch.	Females give birth to a single young. In peninsular Thailand , females with young were found in the maternity roost in April.	This species roosts in caves, crevices, and hollow trees. In peninsular Thailand , the Diadem Leaf-nosed Bat was observed to remain in the cave late, until 20:00 h, being the last species that emerged from the roost Echolocation is a CF/FM type, with a call frequency of the F segment of 58-62 kHz (Malay Peninsula) and 64—66 kHz (Borneo).	The Diadem Leaf-nosed Bat roosts in large colonies in caves. A maternity colony may number several hundred individuals. In southern Myanmar , at least 5000 individuals of this species have been estimated to be sharing a cave with Great Himalayan Leaf-nosed Bats { H. armiger ), Horsfield’s Leaf-nosed Bats ( H. laruatus ), Andersen’s Leaf-nosed Bat (77. gentilis ), Least Leaf-nosed Bats (77. cineraceus ), and Large Long-fingered Bats (Afinio/?tenw magnater).	Classified as Least Concern on IUCN Red List. The Diadem Leaf-nosed Bat is found in several protected areas throughout its range but may be locally at risk due to limestone mining, and quarrying.	Corbet & Hill (1992) | Csorba, Bumrungsri, Francis, Helgen, Bates, Gumal, Kingston et al. (2008) | Francis (2008a) | Pavey & Burwell (1997) | Simmons (2005)		40. Diadem Leaf-nosed Bat Hipposideros diadema French: Phyllorhine à diadème / German: Diadem-Rundblattnase I Spanish: Hiposidérido de diadema Other common names: Diadem Roundleaf Bat Taxonomy. Rhinolophus diadema É. Geoffroy Saint-Hilaire, 1813 , “Timor [Island].” Hipposideros diadema is in the diadema species group. Many subspecies have been described (anderseni, ceramensis, custos, enganus, euotis, griseus, masoni, mirandus, natunensis, nicobarensis, nobilis, oceanitis, reginae, speculator, trobrius, vicarious), several of them of dubious validity; validity, diagnoses, and ranges of prospective subspecies require review. Distribution. Mainland SE Asia, Philippines , Indonesian Archipelago, New Guinea (including Bismarck Archipelago ), Solomon Is, and NE Australia ; also on N Nicobar Is . Descriptive notes. Head—body 66-100 mm, tail 32—51 mm , ear 28—32 mm , hindfoot 16-21 mm, forearm 58—96 mm ; weight 22—57 g . Forearm length can be variable between populations, from as small as 58 mm ( Nicobar Islands ) to as large as 96 mm ( Thailand ). Pelage on upperparts is dark brown with distinctive white or yellowish white patches on shoulders and sides ofback; fur on underparts is grayish white. Noseleafis yellowish brown. Posterior noseleafis thick and tall. There are 3-4 lateral leaflets on each cheek. Skull is heavily built with large canine, inflated rostral swellings and well-developed sagittal crest P2 is small and extruded from tooth row so C1 and P4 are in contact, or almost. Chromosomal complement has 2n = 32 and FN = 60. Habitat. The Diadem Leaf-nosed Bat has been recorded in a wide range of habitats, from lowland primary forest at sea level to agricultural areas and disturbed forests up to 1210 m . Food and Feeding. The Diadem Leaf-nosed Bat forages in forest understory, in gaps, and over streams in forest. It feeds on insects (Coleoptera, Lepidoptera , and various orthopteroids were the most common in fecal pellets) and occasionally on birds. It is known to feed by hanging from a perch and waiting for prey to pass by, then flying to snatch it and returning right away to the perch. Breeding. Females give birth to a single young. In peninsular Thailand , females with young were found in the maternity roost in April. Activity patterns. This species roosts in caves, crevices, and hollow trees. In peninsular Thailand , the Diadem Leaf-nosed Bat was observed to remain in the cave late, until 20:00 h, being the last species that emerged from the roost Echolocation is a CF/FM type, with a call frequency of the F segment of 58-62 kHz (Malay Peninsula) and 64—66 kHz (Borneo). Movements, Home range and Social organization. The Diadem Leaf-nosed Bat roosts in large colonies in caves. A maternity colony may number several hundred individuals. In southern Myanmar , at least 5000 individuals of this species have been estimated to be sharing a cave with Great Himalayan Leaf-nosed Bats { H. armiger ), Horsfield’s Leaf-nosed Bats ( H. laruatus ), Andersen’s Leaf-nosed Bat (77. gentilis ), Least Leaf-nosed Bats (77. cineraceus ), and Large Long-fingered Bats (Afinio/?tenw magnater). Status and Conservation. Classified as Least Concern on IUCN Red List. The Diadem Leaf-nosed Bat is found in several protected areas throughout its range but may be locally at risk due to limestone mining, and quarrying. Bibliography. Corbet & Hill (1992), Csorba, Bumrungsri, Francis, Helgen, Bates, Gumal, Kingston eta/. (2008), Francis (2008a), Pavey & Burwell (1997), Simmons (2005).	Simmons, N.B. and A.L. Cirranello. 2022B. Bat Species of the World: A taxonomic and geographic database. Accessed on 10/11/2022.	Hipposideridae	Hipposideros diadema	Hipposideros		diadema	E. Geoffroy	1813	1	Ann. Mus. Natn. Hist. Nat. Paris	1.016	Diadem Leaf-nosed Bat	<b> ceramensis </b>Laurie and Hill, 1954; <b> custos </b>K. Andersen, 1918; <b> enganus </b>K. Andersen, 1907; <b> euotis </b>K. Andersen, 1905;<b> griseus </b>Meyen, 1883; anderseni Taylor, 1934; pullatus K. Andersen, 1905; <b> masoni </b>Dobson, 1872;<b> mirandus </b>Thomas, 1914; <b> natunensis </b>Chasen, 1940; <b> nicobarensis </b>Dobson, 1871; <b> nobilis </b>Horsfield, 1823; vicarius K. Andersen, 1905; <b> oceanitis </b>K. Andersen, 1905; malaitensis Phillips, 1967;<b> reginae </b>Troughton, 1937; <b> speculator </b>K. Andersen, 1918;<b> trobrius </b>Troughton, 1937.	Indonesia, Lesser Sunda Isls, Timor Isl.	Burma and Vietnam through Thailand, Laos, W Malaysia and Indonesia (including Sumatra, Borneo, and Bali) to New Guinea, Bismarck Arch., Solomon Isls and NE Australia; Philippines; Nicobar Isls. Reports of this species from Cambodia cannot be confirmed (Kock, 2000a).	Not listed.	Least Concern	 diadema species group. Many subspecies are of dubious validity, and several island populations have not been assigned to subspecies. Reviewed in partby Laurie and Hill (1954) and Kitchener et al. (1992b). Does not include demissus and inornatus; see Kitchener et al. (1992b). Alsosee Flannery (1995a, b) and Bonaccorso (1998). Probably includes more than one species; see Esselstyn et al. 2012. May include ornatus, a name listed as a synonym of diadema by Koopman (1993) but which I have been unable to trace (although it may be a lapsus for inornatus). 	Mammal Diversity Database. (2023). Mammal Diversity Database (Version 1.11) [Data set]. Zenodo. https://doi.org/10.5281/zenodo.7830771 released 15 April 2023	Hipposideros diadema	23	Diadem Leaf-nosed Bat	Diadem Roundleaf Bat	Theria	Placentalia	Boreoeutheria	Laurasiatheria	CHIROPTERA	PTEROPODIFORMES	NA	NA	RHINOLOPHOIDEA	HIPPOSIDERIDAE	NA	NA	Hipposideros	NA	diadema	Ã‰. Geoffroy Saint-Hilaire	1813	1	Rhinolophus_diadema	Geoffroy Saint-Hilaire, Ã‰. (1813). Sur un genre de chauve-souris, sous le nom de Rhinolophes (1). Annales du MusÃ©um d'histoire naturelle, 20, 263.	https://www.biodiversitylibrary.org/item/23442#page/283/mode/1up	MNHN 1997-1802		"Timor [Island]."			diadema (Ã‰. Geoffroy Saint-Hilaire, 1813)|nobilis (Horsfield, 1823)|griseus (Meyen, 1833)|nicobarensis (Dobson, 1871)|masoni (Dobson, 1872)|bicarius K. Andersen, 1905|euotis K. Andersen, 1905|oceanitis K. Andersen, 1905|pullatus K. Andersen, 1905|enganus K. Andersen, 1907|mirandus O. Thomas, 1914|custos K. Andersen, 1918|speculator K. Andersen, 1918|anderseni E. H. Taylor, 1934|reginae Troughton, 1937|trobius Troughton, 1937|natunensis Chasen, 1940|ceramensis Laurie & J. Edwards Hill, 1954|malaitensis C. J. Phillips, 1967	NA	NA	Myanmar|Thailand|Laos|Vietnam|Cambodia|Malaysia|Indonesia|Nicobar Islands|Brunei|Philippines|East Timor|Papua New Guinea|Solomon Islands|Australia	Asia|Oceania	Indomalaya|Australasia/Oceania	LC	0	0	0	Hipposideros_diadema	0	sciname match	Hipposideros_diadema	0	IUCN. 2022. The IUCN Red List of Threatened Species. Version 2022-1. https://www.iucnredlist.org. Accessed on [28 September, 2022].	10128	Hipposideros diadema	ANIMALIA	CHORDATA	MAMMALIA	CHIROPTERA	HIPPOSIDERIDAE	Hipposideros	diadema	Geoffroy, 1813	This species is recognized by Simmons and Cirranello (2020) and may have 15 subspecies (Bonaccorso 1998). Additional research is needed to clarify taxonomic relationships and distribution among the subspecies.	20000000	Hipposideros diadema	Least Concern		2021	2021-04-30 00:00:00 UTC	3.1	English	<p>Hipposideros diadema is assessed as Least Concerned as the species does not meet the requirements for a threatened status of the IUCN Red List. It is a widespread species with a broad distribution throughout Southeast Asia, as well as parts of South Asia and Oceania, surpassing the extent of occurrence and area of occupancy requirements to classify as a vulnerable species. There is a presumed large population of H. diadema due to broad distribution. It is suspected to be experiencing a low-level decline due to significant habitat loss and cave disturbances throughout its range, although that decline is unlikely to be at a rate great enough to qualify the species for listing in a threatened category.</p>	<p>The species primarily roosts in caves, but has also been found roosting in buildings, hollow trees, under palms, and underground chambers (Nowak 1999, Francis 2019). Within a crowded cave, H. diadema may roost on walls or near the floor of wet caves (Bonoccorso 1998). In Australia, it was recorded within three different cave types including fully developed tourist caves, self-guided/underdeveloped tourist caves, and non-tourist caves (Pavey 1998). On the Nicobar Islands, it has been recorded in bunkers with a colony size of 20-25, as well as colony sizes greater than 150 within caves (Aul et al. 2014). Maternity colonies of 8,000 H. diadema have been observed in Papua New Guinea (Bonoccorso 1998). Further, it is known to roost with other species in colonies that may reach over 100,000 individuals (Payne et al. 1985). It has been recorded roosting with Rhinolophus affinis at a cave in Penggerukan, North Sumatra (Whitten et al. 2000). In the Philippines, it was found to co-exist with other species in caves including Hipposideros pygmaeus , Rhinolophus arcuatus , Rhinolophus virgo , and Rousettus amplexicaudatus (NuÃ±eza and Galorio 2014), and co-roost with Pipistrellus javanicus (Galorio and NuÃ±eza 2014). Individuals were found to use multiple day roosts but did not change roost every day (Pavey 1998). Ectoparasite loads among H. diadema was recorded to be lowest among individuals within more complex caves and lower densities (Phelps and Kingston 2018), as close contact among females in maternity colonies has been shows to increase parasitism transmission (Christe et al. 2007). It forages in various forested habitats, including highly disturbed areas (Francis 2019). A study in Australia found some flexibility in its foraging ecology, as some individuals occupied up to three types of vegetation including an open forest and vine thicket, although woodland was the most common (Pavey 1998). However, they still required similar habitat components among each type, specifically an area with leafless twigs for perching overlooking an open space. Its wing morphology and high constant echolocation frequency of 59-66kHz are more efficient for foraging in densely vegetated habitats, as higher frequency calls rapidly attenuate in air (Denzinger and Schnitzler 2013). Therefore, they are less effective in locating prey in more open forests or disturbed habitats such as coffee plantations (Kingston 2003, Meijaard 2005). According to Huang et al. (2019), species similar to H. diadema that roost in caves and have higher constant-frequency calls are more tolerant to coffee plantations than plant-roosting species with lower broadband-frequency calls. However, H. diadema is still less likely to be found in an open disturbed habitat such as a coffee plantation, as vegetation simplification decreases prey availability (Wickramasinghe et al. 2004), limits their echolocation efficiency and may increase predation pressure (Gardner 1998). This hypothesis is supported in a study by Huang et al. (2014) that only recorded sightings H. diadema within the primary rainforests of Bukit Barisan Selatan National Park, Sumatra, Indonesia, and only half of the sampled polyculture plantations, while recording no sightings within the sampled disturbed forest and monoculture plantations. Hipposideros diadema is an insectivore, mostly feeding on Coleopterans, Lepidopterans, and Orthopteras, however, it has also been classified as an â€œoccasional carnivoreâ€ that will occasionally feed on small birds and spiders (Pavey and Burwell 1997). Samples of H. diadema stomach contents in Australia consists of 78% Coleoptera and 20% Lepidoptera (Milne et al. 2006). In the Philippines, Galorio and NuÃ±eza (2014) found fruit bits in their stomachs, suggesting they either consumed fruits or the insects attracted to fruits, as bats can echolocate prey that are hidden on a fruit surface (Korine and Kalko 2005). They also found bird feathers and unidentified hair fibers within the stomachs, supporting the theory of occasional carnivory. The species is a perch hunting species, with continuous flight as a secondary behavior (Pavey 1998). It hangs from a perch and scans the area using echolocation until it detects its prey and then makes a fast, direct flight to catch it (Francis 2019). It typically has 1-3 foraging areas with an average foraging range of 1.08km from the day roost (Pavey 1998) but can range up to 10km (Bonoccorso 1998). It also usually goes out for 1-2 foraging bouts per night (Pavey 1998), selecting several perches over 1km<sup>2</sup> (Francis 2019). It has a single breeding season that coincides with warmer temperatures and the maximum quantity of insects (Nowak 1999). The females congregate and form maternity colonies during March and April (Nowak 1998, Francis 2019). In peninsular Thailand, females with young were found in maternity roosts in April (Monadjem et al. 2019). In the southern hemisphere, dependent young and subadult H. diadema were also observed in caves from April through May (Bonoccorso 1998). The females give birth to a single pup and may carry it until it becomes independent enough to fly and feed alone or leave it within the roost when searching for food. Within the Bismarck Archipelago, lactating females are known to carry infants from June through October (Bonoccorso 1998). A young H. diadema will reach sexual maturity after about one year (Nowak 1999). It has an average life span of about four to seven years but can live up to twelve years in captivity (Nowak 1999). ;</p>	<p>Human disturbance and habitat loss (e.g., cave roosts and forest foraging habitats) are the leading threats to H. diadema populations. Caves are the preferred roost site for H. diadema and are highly vulnerable to threats compared to any land resource (Galorio and NuÃ±eza 2014). Such threats include limestone extraction, tourism, guano extraction, and cave swiftlet nests (Galorio and NuÃ±eza 2014, Kingston 2010). Destruction/disturbance of mines has also been shown to significantly threaten cave-roosting species such as H. diadema (Hall et al. 1997). Within Southeast Asia, as much of 74% of forest may be lost by the year 2100 (Sodhi et al. 2004). Singapore has lost 95% of its primary forest since the 1800s with an estimated bat species loss of about 70% (Corlett 1992, Lane et al. 2006). Similarly, the rate of deforestation in Southeast Sulawesi was 41,814 ha/year in 1985â€“1997 (Kuhutanan 2002). Throughout all of Indonesia, the Global Forest Watch reports 27Mha of tree cover loss between 2001-2019 including more than 9.5Mha of humid primary forest, further limiting bat species to protected areas (2021). Hipposideros diadema remains flexible in its utilized foraging habitats, including within highly disturbed areas (Francis 2019). However, the species is still less likely to be found in disturbed habitats and monoculture plantations (Huang et al. 2014) as it is not suited for simplified vegetation, and the expansion of coffee agriculture and other plantations have been shown to significantly reduce both bat abundance and richness (Huang et al. 2019). The increase of such activity will also likely further increase the disturbance of nearby caves, which remains the leading threat to H. diadema populations. Furthermore, simultaneous or continuous stressors, such as habitat loss and human disturbance, can increase vulnerability to pathogens and parasites (Phelps and Kingston 2018). Transmission of parasites through consumption of scavenger insects has also been observed within H. diadema and could post a risk to other population members (Galorio and NuÃ±eza 2014).</p>	<p>Data are limited on the species population size and trend. There is a presumed large population size that is suspected to be experiencing a low-level population decline due to significant habitat loss and cave disturbance. It can be locally common on the Nicobar Islands where colonies of up to 500 bats have been documented (Aul and Vijaykumar 2003, Aul et al. 2014). Furthermore, maternity colonies (females and young) of ca 8,000 H. diadema have been observed in Papua New Guinea (Bonoccorso 1998). There are 15 subspecies recognized, four of which are found in Papua New Guinea (Bonaccorso 1998). The subspecies H. d. masoni on the Andaman Islands which differs from the subspecies H. d. nicobarensis that is endemic to the Nicobar Islands (Srinivasulu et al. 2016). Additional research is needed to clarify the taxonomic relationships among the the subspecies and evaluate if any may warrant elevation to species-level.</p>	Decreasing	The species is widespread and ranges from the Andaman and Nicobar Islands of India of South Asia throughout Southeast Asia and south to northeastern Australia (Srinivasulu et al. 2016, Aul et al. 2014). It is prevalent throughout Southeast Asia including Brunei, Cambodia, East Timor, Indonesia (including Borneo, Sulawesi, Java, Sumatra, and Lesser Sunda Islands), Laos, Malaysia (Peninsular Malaysia and Borneo), Myanmar, Philippines, Thailand, and Vietnam (Huang et al. 2014, Francis 2019, Nowak 1999),the species has not been recorded from Singapore (pers. com. Huang 2021). Within Oceania, it has been recorded in Papua New Guinea, through the Bismarck Archipelago, the Autonomous Region of Bougainville, the Solomon Islands, and as far south as the forests of northeastern Queensland, Australia, (Francis 2019, Nowak 1999). It is found from sea level to 1,300 m asl.	Evidence of hunting of H. diadema include anecdotal reports from Southeast Asia. Since H. diadema is found in many places where bat hunting is common (Aul et al . 2014, Huang et al. 2014, Wiantoro et at . 2016), the species is likely being locally hunted, but there is not enough data to support that it is a major threat to its population.	Terrestrial	<p>Hipposideros diadema is known from protected areas throughout its range and there are currently no known species-specific conservation initiatives in place for the species as it is a Least Concerned species. For example, it has been recorded within and around Bukit Barisan Selatan National Park, Sumatra, Indonesia, which is the second most species rich area in Southeast Asia (Huang et al. 2014). Furthermore, the species was also recorded in areas outside the protection of the national park, including local villages, highlighting the importance of protecting this broader diversity hotspot. Further surveys to identify and protect cave roosts that support the highest populations (Kingston 2010) are needed. Therefore, future management recommendations can focus on effectively providing protection for species as well as maintaining any scientific, cultural, or economic values of caves. Protection of more complex caves would provide more available roost sites for H. diadema , reducing both competition and risk of parasite transmission among individuals. Caves utilized by large maternity colonies should also be identified and protected, as the disturbance of these sites would likely cause local population declines or extirpations. Research on the current population status and trends of H. diadema is lacking, yet crucial in creating effective conservation actions for the species. Similarly, further research on the ecology of maternity roosts would provide more information regarding the impacts of cave disturbance on their population. Huang et al. states that species differ in vulnerability to anthropogenic land use changes (2019), therefore, further species-specific studies must be performed to better analyze species sensitivity and form effective conservation plans. This is especially critical for H. diadema as it is found near many growing plantations/monocultures (Huang 2019, Huang 2014). Lastly, the extent of hunting of H. diadema is unknown and should be quantified to determine its exact impact on their population. Further taxonomic research on the species is needed.</p>	Australasian|Indomalayan		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 	Hipposideridae	Hipposideros		diadema	Ã‰. Geoffroy Saint-Hilaire	1813	1	Ann. Mus. Natn. Hist. Nat. Paris	1.015972	Diadem Leaf-nosed Bat	<b> ceramensis </b>Laurie and Hill, 1954; <b> custos </b>K. Andersen, 1918; <b> enganus </b>K. Andersen, 1907; <b> euotis </b>K. Andersen, 1905;<b> griseus </b>Meyen, 1883; anderseni Taylor, 1934; pullatus K. Andersen, 1905; <b> masoni </b>Dobson, 1872;<b> mirandus </b>Thomas, 1914; <b> natunensis </b>Chasen, 1940; <b> nicobarensis </b>Dobson, 1871; <b> nobilis </b>Horsfield, 1823; vicarius K. Andersen, 1905; <b> oceanitis </b>K. Andersen, 1905; malaitensis Phillips, 1967;<b> reginae </b>Troughton, 1937; <b> speculator </b>K. Andersen, 1918;<b> trobrius </b>Troughton, 1937.	Indonesia, Lesser Sunda Isls, Timor Isl.	Burma and Vietnam through Thailand, Laos, W Malaysia and Indonesia (including Sumatra, Borneo, and Bali) to New Guinea, Bismarck Arch., Solomon Isls and NE Australia; Philippines; Nicobar Isls. Reports of this species from Cambodia cannot be confirmed (Kock, 2000a).	Not listed.	Least Concern	 diadema species group. Many subspecies are of dubious validity, and several island populations have not been assigned to subspecies. Reviewed in partby Laurie and Hill (1954) and Kitchener et al. (1992b). Does not include demissus and inornatus; see Kitchener et al. (1992b). Alsosee Flannery (1995a, b) and Bonaccorso (1998). Probably includes more than one species; see Esselstyn et al. 2012. May include ornatus, a name listed as a synonym of diadema by Koopman (1993) but which I have been unable to trace (although it may be a lapsus for inornatus). 	Hipposideros diadema	1004592	23	Diadem Leaf-nosed Bat	Diadem Roundleaf Bat	Theria	Placentalia	Boreoeutheria	Laurasiatheria	CHIROPTERA	PTEROPODIFORMES	NA	NA	RHINOLOPHOIDEA	Hipposideridae	NA	NA	Hipposideros	NA	diadema	Ã‰. Geoffroy Saint-Hilaire	1813	1	Rhinolophus_diadema	Geoffroy Saint-Hilaire, Ã‰. (1813). Sur un genre de chauve-souris, sous le nom de Rhinolophes (1). Annales du MusÃ©um d'histoire naturelle, 20, 263.	https://www.biodiversitylibrary.org/item/23442#page/283/mode/1up	MNHN 1997-1802		"Timor [Island]."			diadema (Ã‰. Geoffroy Saint-Hilaire, 1813)|nobilis (Horsfield, 1823)|griseus (Meyen, 1833)|nicobarensis (Dobson, 1871)|masoni (Dobson, 1872)|bicarius K. Andersen, 1905|euotis K. Andersen, 1905|oceanitis K. Andersen, 1905|pullatus K. Andersen, 1905|enganus K. Andersen, 1907|mirandus O. Thomas, 1914|custos K. Andersen, 1918|speculator K. Andersen, 1918|anderseni E. H. Taylor, 1934|reginae Troughton, 1937|trobius Troughton, 1937|natunensis Chasen, 1940|ceramensis Laurie & J. Edwards Hill, 1954|malaitensis C. J. Phillips, 1967	NA	NA				Myanmar|Thailand|Laos|Vietnam|Cambodia|Malaysia|Indonesia|Nicobar Islands|Brunei|Philippines|East Timor|Papua New Guinea|Solomon Islands|Australia	Asia|Oceania	Indomalaya|Australasia/Oceania	LC	0	0	0	Hipposideros_diadema	0	sciname match	Hipposideros_diadema	0	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	Hipposideros_diadema	1004592	23	Diadem Roundleaf Bat	Diadem Roundleaf Bat|Diadem Leaf-nosed Bat	Theria	Placentalia	Boreoeutheria	Laurasiatheria	Chiroptera	Yinpterochiroptera	NA	NA	Rhinolophoidea	Hipposideridae	NA	NA	Hipposideros	NA	diadema	Ã‰. Geoffroy Saint-Hilaire	1	Rhinolophus diadema	Geoffroy Saint-Hilaire, Ã‰. 1813. Sur un genre de chauve-souris sous le nom de Rhinolophes. Annales du MusÃ©um d'histoire naturelle 20:254-266.	https://www.biodiversitylibrary.org/page/3553702	MNHN-ZM-MO-1997-1802	holotype	http://coldb.mnhn.fr/catalognumber/mnhn/zm/mo-1997-1802	"Timor [Island]."			NA	NA				Myanmar|Thailand|Laos|Vietnam|Cambodia|Malaysia|Indonesia|Andaman and Nicobar Islands|Brunei|Philippines|East Timor|Papua New Guinea|Solomon Islands|Australia	Asia|Oceania (Continent)	Indomalaya|Australasia	LC	0	0	0	Hipposideros_diadema	0	sciname match	Hipposideros_diadema	0	Simmons, N. B., & Cirranello, A. L. (2025). Batnames.org Species List Version 1.7 (1.7). Zenodo. https://doi.org/10.5281/zenodo.14796586	Hipposideridae	Hipposideros		diadema	Ã‰. Geoffroy Saint-Hilaire	1813	1	Ann. Mus. Natn. Hist. Nat. Paris	1.015972	Diadem Leaf-nosed Bat	ceramensis Laurie and Hill, 1954; custos K. Andersen, 1918; enganus K. Andersen, 1907; euotis K. Andersen, 1905; griseus Meyen, 1883; anderseni Taylor, 1934; pullatus K. Andersen, 1905; masoni Dobson, 1872; mirandus Thomas, 1914; natunensis Chasen, 1940; nicobarensis Dobson, 1871; nobilis Horsfield, 1823; vicarius K. Andersen, 1905; oceanitis K. Andersen, 1905; malaitensis Phillips, 1967; reginae Troughton, 1937; speculator K. Andersen, 1918; trobrius Troughton, 1937.	Indonesia, Lesser Sunda Isls, Timor Isl.	Burma and Vietnam through Thailand, Laos, W Malaysia and Indonesia (including Sumatra, Borneo, and Bali) to New Guinea, Bismarck Arch., Solomon Isls and NE Australia; Philippines; Nicobar Isls. Reports of this species from Cambodia cannot be confirmed (Kock, 2000a).	<a href='https://cites.org/eng/app/appendices.php' target='_blank'>Not Listed</a>	<a href='https://www.iucnredlist.org/species/10128/22095445/' target='_blank'>Least Concern</a>	diademaspecies group. Many subspecies are of dubious validity, and several island populations have not been assigned to subspecies. Reviewed in partby Laurie and Hill (1954) and Kitchener et al. (1992b). Does not include demissus and inornatus; see Kitchener et al. (1992b). Alsosee Flannery (1995a, b) and Bonaccorso (1998). Probably includes more than one species; see Esselstyn et al. 2012. May includeornatus, a name listed as a synonym of diadema by Koopman (1993) but which I have been unable to trace (although it may be a lapsus for inornatus).		Mammal Diversity Database. (2025). Mammal Diversity Database (Version 2.2) [Data set]. Zenodo. https://doi.org/10.5281/zenodo.15007505	NA	Hipposideros diadema; Hipposideros diadema; Hipposideros diadema; Hipposideros diadema; Hipposideros diadema; Hipposideros diadema; diadema; ceramensis; custos; enganus; euotis; griseus; masoni; mirandus; natunensis; nicobarensis; nobilis; oceanitis; reginae; speculator; trobrius; griseus - anderseni; pullatus; nobilis - vicarius; oceanitis - malaitensis; ceramensis; custos; enganus; euotis; griseus; masoni; mirandus; natunensis; nicobarensis; nobilis; oceanitis; reginae; speculator; trobrius; griseus - anderseni; pullatus; nobilis - vicarius; oceanitis - malaitensis; diadema; nobilis; griseus; nicobarensis; masoni; bicarius; euotis; oceanitis; pullatus; enganus; mirandus; custos; speculator; anderseni; reginae; trobius; natunensis; ceramensis; malaitensis; Phyllorhine à diadème; Diadem-Rundblattnase; Hiposidérido de diadema; Diadem Roundleaf Bat; Diadem Leaf-nosed Bat; Diadem Roundleaf Bat; Diadem Leaf-nosed Bat; Diadem Leaf-nosed Bat; H. diadema
