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!/L465	application/vnd.openxmlformats-officedocument.spreadsheetml.sheet	Pipistrellus affinis	Pipistrellus affinis	Pipistrellus affinis	Pipistrellus affinis	Pipistrellus affinis	Falsistrellus affinis	Hypsugo affinis	Hypsugo affinis	Hypsugo affinis	Hypsugo affinis	Hypsugo affinis	Hypsugo affinis	Hypsugo affinis	Hypsugo affinis	Hypsugo affinis		[MSW2] Subgenus Falsistrellus.; [MSW3] May include petersi; see Francis and Hill (1986) and Corbet and Hill (1992). May be conspecific with mordax; see Corbet and Hill (1992). Reviewed by Bates and Harrison (1997).; [HMW] Vesperugo (Pipistrellus) affinis Dobson, 1871 , Bhamo, 1372 m , Kachin State , north-eastern Myanmar . This species, Hypsugo petersi and H. mordax were previously placed in Pipustrellus, where the first two were treated in the “ affinis group” (with some other Asian species) by G. H. H. Tate in 1942, and by K. F. Koopman in 1994. In 1987, based mainly on bacular characters of affinis and petersi ( mordax was not included in the study), J. E. Hill and D. L. Harrison redefined the affinis group, limiting it to these three species ( mordax tentatively), which they placed in the subgenus Falsistrellus of Pipustrellus, alongside the Australian forms tasmaniensis and mackenziei (the tasmaniensis group). G. B. Corbet and Hill followed this arrangement in 1992, whereas in 2005 N. B. Simmons recognized Falsistrellus as a valid genus, with the same five species. The phylogenetic studies of L.. R. Heaney and colleagues in 2012 and M. Ruedi and colleagues in 2017, revealed a close relationship of petersi to Hypsugo . On the basis of sequence data of mitochondrial and nuclear genes, and combining cranial, dental, and multivariate statistical evidence, in 2018 T. Gorfol and G. Csorba (and in 2019 Gorfol and colleagues) recovered petersi within a clade of Hypsugo , with a sister relationship to H. dolichodon; as a result they transferred the Asian members of Falsistrellus ( affinis , mordax , petersi ) to Hypsugo . At the specific level, following Gorfol and Csorba, comparison between specimens of “ affinis ” from Myanmar (Mon State) and Cambodia and those from the Indian subcontinent revealed morphological differences (skull and dental characters, number of caudal vertebrae, bacular form), with the result that the Myanmar and Cambodia specimens were reidentified as H. dolichodon. Earlier, specimens of affinis from India and Sri Lanka had been treated as belonging to mordax . Further studies with genetic data are needed to determine the exact distribution of affinis and its real relationship to mordax and petersi , including whether they are all conspecific (the name mordax has priority), as was previously suspected, for example by C. M. Francis and Hill in 1986 and Corbet and Hill in 1992; comparisons ofthe three are complicated by the fact that mordax is the only one with a type specimen that includes a skull. Gorfol and Csorba also reported that preliminary investigations suggested potentially undescribed forms (unpublished) in the group. Monotypic.; [batnames2022] Formerly included in Falsitrellus ; transferred to Hypsugo by GÃ¶rfÃ¶l and Csorba (2018). May include petersi ; see Francis and Hill (1986) and Corbet and Hill (1992). May be conspecific with mordax ; see Corbet and Hill (1992). Reviewed by Bates and Harrison (1997).; [MDD2022] moved from Falsistrellus to Hypsugo; [IUCN] Earlier forms from India and Sri Lanka were included under Pipistrellus mordax Peters, 1866 (Wroughton 1916, 1918, Ellerman and Morrison-Scott 1951, Phillips 1980), but, are presently considered distinct by Hill and Harrison (1987), Simmons (2005), Srinivasulu and Srinivasulu (2012). This taxon is presently included under the genus Hypsugo Kolenati, 1856 based on statistical and genetic analysis (GÃ¶rfÃ¶l and Csorba 2018), and the genus Falsistrellus Troughton, 1943 sensu stricto is now restricted to Australia.; [batnames2023] Formerly included in Falsitrellus ; transferred to Hypsugo by GÃ¶rfÃ¶l and Csorba (2018). May include petersi ; see Francis and Hill (1986) and Corbet and Hill (1992). May be conspecific with mordax ; see Corbet and Hill (1992). Reviewed by Bates and Harrison (1997).; [MDD2023] moved from Falsistrellus to Hypsugo; [MDD2025_2.0] moved from Falsistrellus to Hypsugo; [batnames2025_1.7] Formerly included in Falsitrellus; transferred to Hypsugo by GÃ¶rfÃ¶l and Csorba (2018). May include petersi; see Francis and Hill (1986) and Corbet and Hill (1992). May be conspecific with mordax; see Corbet and Hill (1992). Reviewed by Bates and Harrison (1997).; [MDD2025_2.2] moved from Falsistrellus to Hypsugo														affinis	Earlier forms from India and Sri Lanka were included under Pipistrellus mordax Peters, 1866 (Wroughton 1916, 1918, Ellerman and Morrison-Scott 1951, Phillips 1980), but, are presently considered distinct by Hill and Harrison (1987), Simmons (2005), Srinivasulu and Srinivasulu (2012). This taxon is presently included under the genus Hypsugo Kolenati, 1856 based on statistical and genetic analysis (GÃ¶rfÃ¶l and Csorba 2018), and the genus Falsistrellus Troughton, 1943 sensu stricto is now restricted to Australia.			affinis 	affinis 			affinis (Dobson, 1871)		Corbet, G.B. and Hill, J.E. 1980. A World List of Mammalian Species. British Museum (Natural History), London, 226 pp.	Chocolate bat	NE Burma, Yunnan	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.	Pipistrellus affinis	Burma, Bhamo.	Dobson	1871	Proc. Asiat. Soc. Bengal, p. 213.	Distribution: Ranging from northern India to southwestern China.		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		India, NE Borneo, Yunnan	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.	Dobson	1871	Proc. Asiat. Soc. Bengal, p. 213.	Subgenus Falsistrellus.	NE Burma, Yunnan (China), N India.	Burma, Bhamo.		DOBSON	1871	Size medium (forearm length, 38-41 mm). Inner upper incisor bicuspid. Outer upper incisor well developed. Anterior upper premolar displaced medially. Rostrum of medium width. Forehead almost flat.	Distribution: Ranging from northern India to southwestern China.	No subspecies.		113	species	P. affinis	DOBSON	1871	Pipistrellus	subgenus	Pipistrellus affinis				Size medium (forearm length, 38-41 mm). Inner upper incisor bicuspid. Outer upper incisor well developed. Anterior upper premolar displaced medially. Rostrum of medium width. Forehead almost flat.	No subspecies.		22. P. affinis (DOBSON 1871) [affinis group].	22	NA			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	Vespertilionidae	Vespertilioninae	Vespertilionini	Falsistrellus affinis	Falsistrellus		affinis	Dobson	y	1871		Proc. Asiat. Soc. Bengal			213		Chocolate Pipistrelle	Burma, Bhamo.	NE Burma, Yunnan (China), India, Nepal, Sri Lanka.	IUCN 2003 and IUCN/SSC Action Plan (2001) – Lower Risk (lc) as Pipistrellus affinus.		May include petersi; see Francis and Hill (1986) and Corbet and Hill (1992). May be conspecific with mordax; see Corbet and Hill (1992). Reviewed by Bates and Harrison (1997).	4C3D87E8FFCD6A72FF4C9E46194AB2E8	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	812	zip:hash://sha256/ec5fd314a06aba1a7b0b72f23e54ac625ae272bd98f82f1d01f4c09627d9e8e0!/treatments-xml-main/data/4C/3D/87/4C3D87E8FFCD6A72FF4C9E46194AB2E8.xml	Hypsugo affinis	Vespertilionidae	Hypsugo	affinis	Dobson	1871	Vespére chocolat @fr | Hochland-Zwergfledermaus @de | Hypsugo chocolatero @es | Grizzled Pipistrelle @en | Highland Pipistrelle @en	Vesperugo (Pipistrellus) affinis Dobson, 1871 , Bhamo, 1372 m , Kachin State , north-eastern Myanmar . This species, Hypsugo petersi and H. mordax were previously placed in Pipustrellus, where the first two were treated in the “ affinis group” (with some other Asian species) by G. H. H. Tate in 1942, and by K. F. Koopman in 1994. In 1987, based mainly on bacular characters of affinis and petersi ( mordax was not included in the study), J. E. Hill and D. L. Harrison redefined the affinis group, limiting it to these three species ( mordax tentatively), which they placed in the subgenus Falsistrellus of Pipustrellus, alongside the Australian forms tasmaniensis and mackenziei (the tasmaniensis group). G. B. Corbet and Hill followed this arrangement in 1992, whereas in 2005 N. B. Simmons recognized Falsistrellus as a valid genus, with the same five species. The phylogenetic studies of L.. R. Heaney and colleagues in 2012 and M. Ruedi and colleagues in 2017, revealed a close relationship of petersi to Hypsugo . On the basis of sequence data of mitochondrial and nuclear genes, and combining cranial, dental, and multivariate statistical evidence, in 2018 T. Gorfol and G. Csorba (and in 2019 Gorfol and colleagues) recovered petersi within a clade of Hypsugo , with a sister relationship to H. dolichodon; as a result they transferred the Asian members of Falsistrellus ( affinis , mordax , petersi ) to Hypsugo . At the specific level, following Gorfol and Csorba, comparison between specimens of “ affinis ” from Myanmar (Mon State) and Cambodia and those from the Indian subcontinent revealed morphological differences (skull and dental characters, number of caudal vertebrae, bacular form), with the result that the Myanmar and Cambodia specimens were reidentified as H. dolichodon. Earlier, specimens of affinis from India and Sri Lanka had been treated as belonging to mordax . Further studies with genetic data are needed to determine the exact distribution of affinis and its real relationship to mordax and petersi , including whether they are all conspecific (the name mordax has priority), as was previously suspected, for example by C. M. Francis and Hill in 1986 and Corbet and Hill in 1992; comparisons ofthe three are complicated by the fact that mordax is the only one with a type specimen that includes a skull. Gorfol and Csorba also reported that preliminary investigations suggested potentially undescribed forms (unpublished) in the group. Monotypic.	India ( Uttarakhand , West Bengal , Maharashtra , Kerala , and Tamil Nadu ), C Nepal , Sri Lanka (Central and Uva provinces), SC China (SE Tibet [= Xizang ], Yunnan , and Guangxi ), and NE Myanmar (known only from type locality in Kachin State ).	Head-body 43-51 mm, tail 30-41 mm, ear 12-15 mm, hindfoot 7-8 mm, forearm 37-8-41-5 mm. Pelage of the Chocolate Pipistrelle is soft, dense, and relatively long; upperparts are chocolate-brown, almost black, lighter on head and neck, with pale gray hairtips, giving slightly grizzled appearance; underparts are also dark,slightly paler than dorsum, with grayish-white bases and dark tips; uniformly white near anus. Wing membranes, ears, and naked parts of face are blackish brown. Ears are broad and rounded, more or less triangular; tragusis broad and pointed at anterior end. Muzzle is moderately long and narrow. Wing membranes attach to base of outertoe. Tail is long, with nine caudal vertebrae. Baculum of a specimen from India is broad, proximally widened and ventrally deeply fluted, with no distal expansion. Skull has relatively low braincase in comparison to rostrum, which is robust and elongated, with lateral and median depressions; forehead is almost flat; zygomata are robust with low but evident postorbital processes; basicranial pits are poorly developed; coronoid process of each half mandible exceeds C, in height. I? is short and broad; I* is well developed, equal in height to secondary cusp of I*, and with distinct accessory cusp internally; it is usually situated closely adjacent to C', which is unicuspid and broad at base; P* is of moderate size, subequal to I” in crown area and slightly displaced internally; C! and P* are not in contact, according to specimens from India , but in specimens from China they be may slightly in contact; P,is situated in tooth row, and is about two-thirds the crown area and height of P,. Condilo-canine lengths are 13-7-14-5 mm, and maxillary tooth row lengths are 5-5 7 mm . In 1969, S. Pathak and T. Sharma reported two different karyotypes under different names from the same locality in India ( Maharashtra ), 2n = 36 and FN = 50 for the form then named Pipustrellus affinis , and 2n = 34 and FN = 46 for P. mordax ; they differ by a small pair of subtelocentric chromosomes.	The Chocolate Pipistrelle is apparently confined to high altitudes up to ¢. 2000 m . In Sri Lanka , it has been recorded in Central Highlands at 1846 m , in Nepal at 2000 m , and in Darjeeling district, India , at 1452 m . In Myanmar ,it was recorded in Bhamo, a town beside the Irrawaddy River surrounded by deciduous and evergreen forest.	Chocolate Pipistrellesfly at heights of 5-6 m and catch small flying insects such as mosquitoes.	No information.	The Chocolate Pipistrelle is nocturnal. It appears to spend the day in the roofs of buildings or in cracks and small holes in tree trunks, emerging at dusk to feed on insects, which it captures around human habitations and clearings. It may hibernate for a short period during cold and frosty weather.	Chocolate Pipistrelles roost in small colonies of 5-6 individuals.	Classified as Least Concern on The IUCN Red List (as Falsistrellus affinis ),, in view ofits wide distribution and expected large population, and because it is unlikely to be declining quickly. In parts of South Asia, the Chocolate Pipistrelle is threatened by habitat loss, largely through commercial logging and conversion of land for agriculture, as well as human interference at roosting sites. Further studies are needed into its taxonomy, distribution, abundance, reproduction, and ecology.	Acharya et al. (2010) | Bates & Harrison (1997) | Bates et al. (2005) | Boitani et al. (2006) | Chheang et al. (2013) | Corbet & Hill (1992) | Csorba, Bumrungsri, Francis, Bates, Gumal & Kingston (2008f) | Das (2003) | Dobson (1871b) | Ellerman & Morrison-Scott (1951) | Francis (2008a) | Francis & Hill (1986) | Gorfol & Csorba (2018) | Gorfol, Csorba et al. (2014) | Gorfol, Furey et al. (2019) | Heaney et al. (2012) | Hill & Harrison (1987) | Koopman (1994) | Molur et al. (2002) | Pathak & Sharma (1969) | Phauk et al. (2013) | Phillips (1980) | Ruedi, Eger et al. (2017) | Simmons (2005) | Smith & Xie Yan (2008) | Srinivasulu & Srinivasulu (2012) | Tate (1942b) | Wroughton (1916, 1918a) | Yapa & Ratnavira (2013)	https://zenodo.org/record/6397984/files/figure.png	102. Chocolate Pipistrelle Hypsugo affinis French: Vespére chocolat / German: Hochland-Zwergfledermaus / Spanish: Hypsugo chocolatero Other common names: Grizzled Pipistrelle , Highland Pipistrelle Taxonomy. Vesperugo (Pipistrellus) affinis Dobson, 1871 , Bhamo, 1372 m , Kachin State , north-eastern Myanmar . This species, Hypsugo petersi and H. mordax were previously placed in Pipustrellus, where the first two were treated in the “ affinis group” (with some other Asian species) by G. H. H. Tate in 1942, and by K. F. Koopman in 1994. In 1987, based mainly on bacular characters of affinis and petersi ( mordax was not included in the study), J. E. Hill and D. L. Harrison redefined the affinis group, limiting it to these three species ( mordax tentatively), which they placed in the subgenus Falsistrellus of Pipustrellus, alongside the Australian forms tasmaniensis and mackenziei (the tasmaniensis group). G. B. Corbet and Hill followed this arrangement in 1992, whereas in 2005 N. B. Simmons recognized Falsistrellus as a valid genus, with the same five species. The phylogenetic studies of L.. R. Heaney and colleagues in 2012 and M. Ruedi and colleagues in 2017, revealed a close relationship of petersi to Hypsugo . On the basis of sequence data of mitochondrial and nuclear genes, and combining cranial, dental, and multivariate statistical evidence, in 2018 T. Gorfol and G. Csorba (and in 2019 Gorfol and colleagues) recovered petersi within a clade of Hypsugo , with a sister relationship to H. dolichodon; as a result they transferred the Asian members of Falsistrellus ( affinis , mordax , petersi ) to Hypsugo . At the specific level, following Gorfol and Csorba, comparison between specimens of “ affinis ” from Myanmar (Mon State) and Cambodia and those from the Indian subcontinent revealed morphological differences (skull and dental characters, number of caudal vertebrae, bacular form), with the result that the Myanmar and Cambodia specimens were reidentified as H. dolichodon. Earlier, specimens of affinis from India and Sri Lanka had been treated as belonging to mordax . Further studies with genetic data are needed to determine the exact distribution of affinis and its real relationship to mordax and petersi , including whether they are all conspecific (the name mordax has priority), as was previously suspected, for example by C. M. Francis and Hill in 1986 and Corbet and Hill in 1992; comparisons ofthe three are complicated by the fact that mordax is the only one with a type specimen that includes a skull. Gorfol and Csorba also reported that preliminary investigations suggested potentially undescribed forms (unpublished) in the group. Monotypic. Distribution. India ( Uttarakhand , West Bengal , Maharashtra , Kerala , and Tamil Nadu ), C Nepal , Sri Lanka (Central and Uva provinces), SC China (SE Tibet [= Xizang ], Yunnan , and Guangxi ), and NE Myanmar (known only from type locality in Kachin State ). Descriptive notes. Head-body 43-51 mm, tail 30-41 mm, ear 12-15 mm, hindfoot 7-8 mm, forearm 37-8-41-5 mm. Pelage of the Chocolate Pipistrelle is soft, dense, and relatively long; upperparts are chocolate-brown, almost black, lighter on head and neck, with pale gray hairtips, giving slightly grizzled appearance; underparts are also dark,slightly paler than dorsum, with grayish-white bases and dark tips; uniformly white near anus. Wing membranes, ears, and naked parts of face are blackish brown. Ears are broad and rounded, more or less triangular; tragusis broad and pointed at anterior end. Muzzle is moderately long and narrow. Wing membranes attach to base of outertoe. Tail is long, with nine caudal vertebrae. Baculum of a specimen from India is broad, proximally widened and ventrally deeply fluted, with no distal expansion. Skull has relatively low braincase in comparison to rostrum, which is robust and elongated, with lateral and median depressions; forehead is almost flat; zygomata are robust with low but evident postorbital processes; basicranial pits are poorly developed; coronoid process of each half mandible exceeds C, in height. I? is short and broad; I* is well developed, equal in height to secondary cusp of I*, and with distinct accessory cusp internally; it is usually situated closely adjacent to C', which is unicuspid and broad at base; P* is of moderate size, subequal to I” in crown area and slightly displaced internally; C! and P* are not in contact, according to specimens from India , but in specimens from China they be may slightly in contact; P,is situated in tooth row, and is about two-thirds the crown area and height of P,. Condilo-canine lengths are 13-7-14-5 mm, and maxillary tooth row lengths are 5-5 7 mm . In 1969, S. Pathak and T. Sharma reported two different karyotypes under different names from the same locality in India ( Maharashtra ), 2n = 36 and FN = 50 for the form then named Pipustrellus affinis , and 2n = 34 and FN = 46 for P. mordax ; they differ by a small pair of subtelocentric chromosomes. Habitat. The Chocolate Pipistrelle is apparently confined to high altitudes up to ¢. 2000 m . In Sri Lanka , it has been recorded in Central Highlands at 1846 m , in Nepal at 2000 m , and in Darjeeling district, India , at 1452 m . In Myanmar ,it was recorded in Bhamo, a town beside the Irrawaddy River surrounded by deciduous and evergreen forest. Food and Feeding. Chocolate Pipistrellesfly at heights of 5-6 m and catch small flying insects such as mosquitoes. Breeding. No information. Activity patterns. The Chocolate Pipistrelle is nocturnal. It appears to spend the day in the roofs of buildings or in cracks and small holes in tree trunks, emerging at dusk to feed on insects, which it captures around human habitations and clearings. It may hibernate for a short period during cold and frosty weather. Movements, Home range and Social organization. Chocolate Pipistrelles roost in small colonies of 5-6 individuals. Status and Conservation. Classified as Least Concern on The IUCN Red List (as Falsistrellus affinis ),, in view ofits wide distribution and expected large population, and because it is unlikely to be declining quickly. In parts of South Asia, the Chocolate Pipistrelle is threatened by habitat loss, largely through commercial logging and conversion of land for agriculture, as well as human interference at roosting sites. Further studies are needed into its taxonomy, distribution, abundance, reproduction, and ecology. Bibliography. Acharya et al. (2010), Bates & Harrison (1997), Bates et al. (2005), Boitani et al. (2006), Chheang et al. (2013), Corbet & Hill (1992), Csorba, Bumrungsri, Francis, Bates, Gumal & Kingston (2008f), Das (2003), Dobson (1871b), Ellerman & Morrison-Scott (1951), Francis (2008a), Francis & Hill (1986), Gorfol & Csorba (2018), Gorfol, Csorba et al. (2014), Gorfol, Furey et al. (2019), Heaney et al. (2012), Hill & Harrison (1987), Koopman (1994), Molur et al. (2002), Pathak & Sharma (1969), Phauk et al. (2013), Phillips (1980), Ruedi, Eger et al. (2017), Simmons (2005), Smith & Xie Yan (2008), Srinivasulu & Srinivasulu (2012), Tate (1942b), Wroughton (1916, 1918a), Yapa & Ratnavira (2013).	Simmons, N.B. and A.L. Cirranello. 2022B. Bat Species of the World: A taxonomic and geographic database. Accessed on 10/11/2022.	Vespertilionidae	Hypsugo affinis	Hypsugo		affinis	Dobson	1871	1	Proc. Asiat. Soc. Bengal	1874:33:00	Chocolate Pipistrelle	None.	Burma, Bhamo.	NE Burma, Yunnan (China), India, Nepal, Sri Lanka.	Not listed.	Least Concern	Formerly included in Falsitrellus ; transferred to Hypsugo by GÃ¶rfÃ¶l and Csorba (2018). May include petersi ; see Francis and Hill (1986) and Corbet and Hill (1992). May be conspecific with mordax ; see Corbet and Hill (1992). Reviewed by Bates and Harrison (1997).	Mammal Diversity Database. (2023). Mammal Diversity Database (Version 1.11) [Data set]. Zenodo. https://doi.org/10.5281/zenodo.7830771 released 15 April 2023	Hypsugo affinis	23	Chocolate Pipistrelle	Grizzled Pipistrelle|Highland Pipistrelle	Theria	Placentalia	Boreoeutheria	Laurasiatheria	CHIROPTERA	VESPERTILIONIFORMES	NA	NA	VESPERTILIONOIDEA	VESPERTILIONIDAE	VESPERTILIONINAE	VESPERTILIONINI	Hypsugo	NA	affinis	Dobson	1871	1	Pipistrellus_affinis	Dobson, G. E. (1871). Notes on nine new species of Indian and Indo-Chinese Vespertilionidae, with remarks on the synonymy and classification of some other species of the same family. Proceedings of the Asiatic Society of Bengal, 1871, 213.	https://www.biodiversitylibrary.org/item/44923#page/259/mode/1up	ZSI 15592		Bhamo, 1372 m, Kachin State, north-eastern Myanmar.			affinis (Dobson, 1871)	moved from Falsistrellus to Hypsugo	GÃ³rfÃ³l, T., & Csorba, G. (2018). Integrative taxonomy places Asian species of Falsistrellus (Chiroptera: Vespertilionidae) into Hypsugo. Mammalian Biology, 93(1), 56-63.	India|Nepal|Sri Lanka|China|Myanmar	Asia	Indomalaya|Palearctic	LC	0	0	0	Hypsugo_affinis	0	sciname match	Falsistrellus_affinis	0	IUCN. 2022. The IUCN Red List of Threatened Species. Version 2022-1. https://www.iucnredlist.org. Accessed on [28 September, 2022].	17324	Hypsugo affinis	ANIMALIA	CHORDATA	MAMMALIA	CHIROPTERA	VESPERTILIONIDAE	Hypsugo	affinis	Dobson, 1871	Earlier forms from India and Sri Lanka were included under Pipistrellus mordax Peters, 1866 (Wroughton 1916, 1918, Ellerman and Morrison-Scott 1951, Phillips 1980), but, are presently considered distinct by Hill and Harrison (1987), Simmons (2005), Srinivasulu and Srinivasulu (2012). This taxon is presently included under the genus Hypsugo Kolenati, 1856 based on statistical and genetic analysis (GÃ¶rfÃ¶l and Csorba 2018), and the genus Falsistrellus Troughton, 1943 sensu stricto is now restricted to Australia.	20000000	Hypsugo affinis	Least Concern		2019	2018-08-31 00:00:00 UTC	3.1	English	Confirmed as Least Concern in view of its wide distribution, presumed large population, and because it is unlikely to be declining fast enough to qualify for listing in a more threatened category.	This species roosts in small colonies of five or six individuals in roofs of buildings and cracks, hollows in trees, near human habitations (Molur et al. 2002, Smith and Xie 2008). It feeds on small insects flying low near the ground and seen near human habitation (Bates and Harrison 1997, Smith and Xie 2008).	There are no major threats to this species in Southeast Asia. In parts of South Asia, this species is threatened by habitat loss, largely through commercial logging and the conversion of land to agricultural use and human interference to roosting sites (Molur et al . 2002).	There is little information about the abundance of this species. Though widely distributed in South Asia, the population size is believed to be small and a declining trend in the population is inferred (Molur et al. 2002).	Unknown	This species is generally distributed in southern and northern parts of South Asia, southern China, and western Southeast Asia. In South Asia, it is known from India (Kerala, Maharashtra, Tamil Nadu, Uttarakhand and West Bengal), Nepal (Central Nepal) and Sri Lanka (Central and Uva provinces). In China, it has been recorded from Xizang, Yunnan, and Guangxi (Smith and Xie 2008). In Southeast Asia, it appears to have only been recorded from NE Myanmar (Smith and Xie 2008). It ranges from sea level up to around 2,000 m asl.		Terrestrial	In South Asia, there are no conservation measures in place and this species has not been recorded from any protected areas.	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 	Vespertilionidae	Hypsugo		affinis	Dobson	1871	1	Proc. Asiat. Soc. Bengal	1874:33:00	Chocolate Pipistrelle	None.	Burma, Bhamo.	NE Burma, Yunnan (China), India, Nepal, Sri Lanka.	Not listed.	Least Concern	Formerly included in Falsitrellus ; transferred to Hypsugo by GÃ¶rfÃ¶l and Csorba (2018). May include petersi ; see Francis and Hill (1986) and Corbet and Hill (1992). May be conspecific with mordax ; see Corbet and Hill (1992). Reviewed by Bates and Harrison (1997).	Hypsugo affinis	1005712	23	Chocolate Pipistrelle	Grizzled Pipistrelle|Highland Pipistrelle	Theria	Placentalia	Boreoeutheria	Laurasiatheria	CHIROPTERA	VESPERTILIONIFORMES	NA	NA	VESPERTILIONOIDEA	Vespertilionidae	VESPERTILIONINAE	VESPERTILIONINI	Hypsugo	NA	affinis	Dobson	1871	1	Pipistrellus_affinis	Dobson, G. E. (1871). Notes on nine new species of Indian and Indo-Chinese Vespertilionidae, with remarks on the synonymy and classification of some other species of the same family. Proceedings of the Asiatic Society of Bengal, 1871, 213.	https://www.biodiversitylibrary.org/item/44923#page/259/mode/1up	ZSI 15592		Bhamo, 1372 m, Kachin State, north-eastern Myanmar.			affinis (Dobson, 1871)	moved from Falsistrellus to Hypsugo	GÃ³rfÃ³l, T., & Csorba, G. (2018). Integrative taxonomy places Asian species of Falsistrellus (Chiroptera: Vespertilionidae) into Hypsugo. Mammalian Biology, 93(1), 56-63.				India|Nepal|Sri Lanka|China|Myanmar	Asia	Indomalaya|Palearctic	LC	0	0	0	Hypsugo_affinis	0	sciname match	Falsistrellus_affinis	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	Hypsugo_affinis	1005712	23	Chocolate Pipistrelle	Grizzled Pipistrelle|Highland Pipistrelle	Theria	Placentalia	Boreoeutheria	Laurasiatheria	Chiroptera	Yangochiroptera	NA	NA	Vespertilionoidea	Vespertilionidae	Vespertilioninae	Vespertilionini	Hypsugo	NA	affinis	Dobson	1	Pipistrellus affinis	Dobson, G.E. 1871. Notes on nine new species of Indian and Indo-Chinese Vespertilionidae, with remarks on the synonymy and classification of some other species of the same family. Proceedings of the Asiatic Society of Bengal 1871:210-215.	https://www.biodiversitylibrary.org/page/12393595	ZSI 15592	holotype		Bhamo, 1372 m, Kachin State, north-eastern Myanmar.			moved from Falsistrellus to Hypsugo	GÃ³rfÃ³l, T., & Csorba, G. (2018). Integrative taxonomy places Asian species of Falsistrellus (Chiroptera: Vespertilionidae) into Hypsugo. Mammalian Biology, 93(1), 56-63.				India|Nepal|Sri Lanka|China|Myanmar	Asia	Indomalaya|Palearctic	LC	0	0	0	Hypsugo_affinis	0	sciname match	Falsistrellus_affinis	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	Vespertilionidae	Hypsugo		affinis	Dobson	1871	1	Proc. Asiat. Soc. Bengal	1874:33:00	Chocolate Pipistrelle	None.	Burma, Bhamo.	NE Burma, Yunnan (China), India, Nepal, Sri Lanka.	<a href='https://cites.org/eng/app/appendices.php' target='_blank'>Not Listed</a>	<a href='https://www.iucnredlist.org/species/17324/22131594/' target='_blank'>Least Concern</a>	Formerly included in Falsitrellus; transferred to Hypsugo by GÃ¶rfÃ¶l and Csorba (2018). May include petersi; see Francis and Hill (1986) and Corbet and Hill (1992). May be conspecific with mordax; see Corbet and Hill (1992). Reviewed by Bates and Harrison (1997).		Mammal Diversity Database. (2025). Mammal Diversity Database (Version 2.2) [Data set]. Zenodo. https://doi.org/10.5281/zenodo.15007505	NA	Falsistrellus affinis; Hypsugo affinis; Hypsugo affinis; Hypsugo affinis; Hypsugo affinis; Hypsugo affinis; affinis; Vespére chocolat; Hochland-Zwergfledermaus; Hypsugo chocolatero; Grizzled Pipistrelle; Highland Pipistrelle; Chocolate Pipistrelle; Grizzled Pipistrelle; Highland Pipistrelle; Chocolate Pipistrelle; Chocolate Pipistrelle; Pipistrellus affinis; H. affinis
