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!/L160	application/vnd.openxmlformats-officedocument.spreadsheetml.sheet	N/A	Eptesicus bottae [synonym of]	N/A	Eptesicus bottae [synonym of]	Eptesicus bottae anatolicus	Eptesicus bottae anatolicus	Eptesicus anatolicus	Eptesicus anatolicus	Eptesicus anatolicus	Eptesicus anatolicus	Eptesicus anatolicus	Eptesicus anatolicus	Cnephaeus anatolicus	Cnephaeus anatolicus	Cnephaeus anatolicus		[HMW] Eplesicus anatolicus Felten, 1971 , Alanya, Antalya , Turkey . Eptesicus anatolicus was previously included as a subspecies of E. bottae , but genetic and morphological data suggest that E. anatolicus is a distinct species. According to genetic data presented byJ. Juste and colleagues in 2013,it is either sister to a clade including E. pachyomus , a paraphyletic E. serotinus , E. ognevi , and E. bottae (using mitochondrial genes) or is in a clade with E. ognevi , E. hottentotus , and E. bottae (using nuclear genes). Nevertheless, I. V. Artyushin and col leagues in 2018 found a similarly conflicting dataset that supported the traditional view that E. bottae includes both E. ogneuvi and E. anatolicus based on nuclear genes. Eptesicus ognevi and E. anatolicus are 1ncluded as distinct species here, pending a more complete genetic and morphological study encompassing the full distributions of all taxa in E. bottae sensu lato . Eptesicus anatolicus might be found sympatrically with E. ognevi in the southern Caucasus. Monotypic.; [batnames2022] Subgenus Cnephaeus . Distinct from bottae; see Han&aacute;k et al. (2001), Benda et al. (2006), Mayer et al. (2007), and Juste et al. (2012). May contain additional cryptic diversity see Juste et al. (2012).; [MDD2022] split from E. bottae; [IUCN] In previous Red List assessments, Eptesicus anatolicus was included within E. bottae . It is now considered a separate species (Benda et al. 2006, Juste et al. 2013, Artyushin et al. 2018).; [batnames2023] Subgenus Cnephaeus . Distinct from bottae; see Han&aacute;k et al. (2001), Benda et al. (2006), Mayer et al. (2007), and Juste et al. (2012). May contain additional cryptic diversity see Juste et al. (2012).; [MDD2023] split from E. bottae; [MDD2025_2.0] split from E. bottae; moved from Eptesicus to Cnephaeus; [batnames2025_1.7] Distinct from bottae; see Han&aacute;k et al. (2001), Benda et al. (2006), Mayer et al. (2007), and Juste et al. (2012). May contain additional cryptic diversity see Juste et al. (2012).; [MDD2025_2.2] split from E. bottae; moved from Eptesicus to Cnephaeus														anatolicus	In previous Red List assessments, Eptesicus anatolicus was included within E. bottae . It is now considered a separate species (Benda et al. 2006, Juste et al. 2013, Artyushin et al. 2018).			anatolicus	anatolicus			anatolicus (Felten, 1971)						N/A																																								NA																											4C3D87E8FFA16A1EFF429DAD16F3B09B	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	848	zip:hash://sha256/ec5fd314a06aba1a7b0b72f23e54ac625ae272bd98f82f1d01f4c09627d9e8e0!/treatments-xml-main/data/4C/3D/87/4C3D87E8FFA16A1EFF429DAD16F3B09B.xml	Eptesicus anatolicus	Vespertilionidae	Eptesicus	anatolicus	Felten	1971	Sérotine d'Anatolie @fr | Anatolien-Breitflligelfledermaus @de | Eptesicus de Anatolia @es | Anatolian Serotine Bat @en	Eplesicus anatolicus Felten, 1971 , Alanya, Antalya , Turkey . Eptesicus anatolicus was previously included as a subspecies of E. bottae , but genetic and morphological data suggest that E. anatolicus is a distinct species. According to genetic data presented byJ. Juste and colleagues in 2013,it is either sister to a clade including E. pachyomus , a paraphyletic E. serotinus , E. ognevi , and E. bottae (using mitochondrial genes) or is in a clade with E. ognevi , E. hottentotus , and E. bottae (using nuclear genes). Nevertheless, I. V. Artyushin and col leagues in 2018 found a similarly conflicting dataset that supported the traditional view that E. bottae includes both E. ogneuvi and E. anatolicus based on nuclear genes. Eptesicus ognevi and E. anatolicus are 1ncluded as distinct species here, pending a more complete genetic and morphological study encompassing the full distributions of all taxa in E. bottae sensu lato . Eptesicus anatolicus might be found sympatrically with E. ognevi in the southern Caucasus. Monotypic.	Rhodes I ( Greece ), S Turkey , NE Cyprus , N Syria , Lebanon , N & E Iraq , and W & S Iran .	Head—body 66-72 mm, tail 49-57 mm, ear 18-4-20-6 mm, forearm 46-1-50-4 mm; weight 14-3 g. Dorsal pelage of the Anatolian Serotine is light to dark creamy buff, with rusty brown to brownish gray tinge; ventral pelage is whitish beige. Bare parts of face, ears, membranes, and limbs are dark brown to blackish brown. Ears are relatively short and subtriangular, with roundedtips; tragus is ¢.50% the ear length and same width from base to tip, with rounded tip. Wings and uropatagium are semitranslucent, and tail protrudes c.3-5 mm past uropatagium; postcalcarial lobe is well developed. Baculum is larger (0-97-12 mm long) and more massive than in Botta’ Serotine ( E. bottae ) and is Y-shaped (base with moderately deep bifurcation, less so than in the Eurasian Serotine, E. serotinus , that has similarly shaped baculum) rather than triangular. Compared with Botta’s Serotine, the Anatolian Serotine has broader and more robust skull and more massive braincase overall; craniodental characteristics are otherwise similar to Botta’s Serotine. Chromosomal complement has 2n = 50, FNa = 48, and FN = 52 (Rhodes Island and Turkey ).	Arid and semiarid deserts, steppes, and rocky areas, generally not far from water, but also dry forested and temperate habitats, such as deciduous steppe forest climaxes in Iraq and Iran , and Mediterranean woodland climax and steppe-maquis areas in the Levant region and Turkey , from sea level to elevations of more than 1850 m . Anatolian Serotines are found in highlands of the Zagros Mountainsin Iran and primarily in lowlands in Lebanon (mean elevation of 338-8 m and maximum of 1025 m ) and Syria (10-370 m).	Anatolian Serotines forage by slow hawking in open and semi-open areas along cliffs and vegetation and around streetlamps. They appear to feed rather opportunistically on various insects. In Syria , two sample sets offeces contained mostly Hymenoptera (Formicoidea) ; another two sets of digestive tracts contained mainly Diptera (Brachycera) , followed by Heteroptera. In Turkey , Coleoptera (particularly Carabidae ) were the most prominent in diets. A single sample from Rhodes Island contained mostly Hymenoptera , and a sample from Lebanon included mostly Coleoptera , Hymenoptera , and Heteroptera. Three digestive tracts of bats in Iran contained Coleoptera (40% by volume), Orthoptera (25%), Lepidoptera (20%), Neuroptera (10%), and Hemiptera ( Aphididae ; 5%), and two fecal pellets contained Odonata (60%) and Hymenoptera (Formicoidea; 40%).	In Syria , one postpartum Anatolian Serotine and four pregnant females were caught in late May. Each of pregnant female had two fetuses. A nearly full-grown young roosting with its mother was captured in July in Syria . Births in Syria likely occur in May-June, which might be true in Lebanon because a pregnant female with two fetuses was caught in early June and young in mid-July.	Day roosts have been found in crevices between bricks and stones in buildings, and some individuals have been netted at entrances of caves, suggesting that they roost in caves. Search-call shape is FM/QCF sweep. Calls in Iran had peak frequencies of 28:9-29-1 kHz. On Rhodes Island,start frequencies were ¢.29-32 kHz, and end frequencies were ¢.27-28 kHz.	The Anatolian Serotine appears to roost in colonies of 1-3 individuals. In Turkey , maternity colonies with 15-20 individuals and solitary individuals of both sexes, females occasionally having young, have been found. In Syria , Anatolian Serotines shared roosts with Savi’s Pipistrelles ( Hypsugo savii ), Greater Horseshoe Bats (Rhinolophus ferrumequinum), Lesser Myotis ( Myotis blythii ), Greater Myotis ( M. myotis ), and Natterer’s Myotis ( M. nattereri ).	Not assessed on The IUCN Red List. The Anatolian Serotine is included under Botta’s Serotine, which is classified as Least Concern. Little is known regarding its ecology and threats, but it appears to be relatively widespread and is common around the eastern Mediterranean.	Artyushin, Bannikova et al. (2009) | Artyushin, Kruskop et al. (2018) | Aulagnier et al. (2008) | Benda, Abi-Said et al. (2016) | Benda, Andreas et al. (2006) | Benda, Hanék et al. (2007) | Benda, Lucan et al. (2010) | Dietz et al. (2007) | Felten (1971) | von Helversen (1998) | Juste et al. (2013) | Karatas & Sézen (2007) | Mayeret al. (2007) | Shehab et al. (2007) | Volleth et al. (2001) | Whitaker & Karatas (2009)	https://zenodo.org/record/6398212/files/figure.png	192. Anatolian Serotine Eptesicus anatolicus French: Sérotine d'Anatolie / German: Anatolien-Breitflligelfledermaus / Spanish: Eptesicus de Anatolia Other common names: Anatolian Serotine Bat Taxonomy. Eplesicus anatolicus Felten, 1971 , Alanya, Antalya , Turkey . Eptesicus anatolicus was previously included as a subspecies of E. bottae , but genetic and morphological data suggest that E. anatolicus is a distinct species. According to genetic data presented byJ. Juste and colleagues in 2013,it is either sister to a clade including E. pachyomus , a paraphyletic E. serotinus , E. ognevi , and E. bottae (using mitochondrial genes) or is in a clade with E. ognevi , E. hottentotus , and E. bottae (using nuclear genes). Nevertheless, I. V. Artyushin and col leagues in 2018 found a similarly conflicting dataset that supported the traditional view that E. bottae includes both E. ogneuvi and E. anatolicus based on nuclear genes. Eptesicus ognevi and E. anatolicus are 1ncluded as distinct species here, pending a more complete genetic and morphological study encompassing the full distributions of all taxa in E. bottae sensu lato . Eptesicus anatolicus might be found sympatrically with E. ognevi in the southern Caucasus. Monotypic. Distribution. Rhodes I ( Greece ), S Turkey , NE Cyprus , N Syria , Lebanon , N & E Iraq , and W & S Iran . Descriptive notes. Head—body 66-72 mm, tail 49-57 mm, ear 18-4-20-6 mm, forearm 46-1-50-4 mm; weight 14-3 g. Dorsal pelage of the Anatolian Serotine is light to dark creamy buff, with rusty brown to brownish gray tinge; ventral pelage is whitish beige. Bare parts of face, ears, membranes, and limbs are dark brown to blackish brown. Ears are relatively short and subtriangular, with roundedtips; tragus is ¢.50% the ear length and same width from base to tip, with rounded tip. Wings and uropatagium are semitranslucent, and tail protrudes c.3-5 mm past uropatagium; postcalcarial lobe is well developed. Baculum is larger (0-97-12 mm long) and more massive than in Botta’ Serotine ( E. bottae ) and is Y-shaped (base with moderately deep bifurcation, less so than in the Eurasian Serotine, E. serotinus , that has similarly shaped baculum) rather than triangular. Compared with Botta’s Serotine, the Anatolian Serotine has broader and more robust skull and more massive braincase overall; craniodental characteristics are otherwise similar to Botta’s Serotine. Chromosomal complement has 2n = 50, FNa = 48, and FN = 52 (Rhodes Island and Turkey ). Habitat. Arid and semiarid deserts, steppes, and rocky areas, generally not far from water, but also dry forested and temperate habitats, such as deciduous steppe forest climaxes in Iraq and Iran , and Mediterranean woodland climax and steppe-maquis areas in the Levant region and Turkey , from sea level to elevations of more than 1850 m . Anatolian Serotines are found in highlands of the Zagros Mountainsin Iran and primarily in lowlands in Lebanon (mean elevation of 338-8 m and maximum of 1025 m ) and Syria (10-370 m). Food and Feeding. Anatolian Serotines forage by slow hawking in open and semi-open areas along cliffs and vegetation and around streetlamps. They appear to feed rather opportunistically on various insects. In Syria , two sample sets offeces contained mostly Hymenoptera (Formicoidea) ; another two sets of digestive tracts contained mainly Diptera (Brachycera) , followed by Heteroptera. In Turkey , Coleoptera (particularly Carabidae ) were the most prominent in diets. A single sample from Rhodes Island contained mostly Hymenoptera , and a sample from Lebanon included mostly Coleoptera , Hymenoptera , and Heteroptera. Three digestive tracts of bats in Iran contained Coleoptera (40% by volume), Orthoptera (25%), Lepidoptera (20%), Neuroptera (10%), and Hemiptera ( Aphididae ; 5%), and two fecal pellets contained Odonata (60%) and Hymenoptera (Formicoidea; 40%). Breeding. In Syria , one postpartum Anatolian Serotine and four pregnant females were caught in late May. Each of pregnant female had two fetuses. A nearly full-grown young roosting with its mother was captured in July in Syria . Births in Syria likely occur in May-June, which might be true in Lebanon because a pregnant female with two fetuses was caught in early June and young in mid-July. Activity patterns. Day roosts have been found in crevices between bricks and stones in buildings, and some individuals have been netted at entrances of caves, suggesting that they roost in caves. Search-call shape is FM/QCF sweep. Calls in Iran had peak frequencies of 28:9-29-1 kHz. On Rhodes Island,start frequencies were ¢.29-32 kHz, and end frequencies were ¢.27-28 kHz. Movements, Home range and Social organization. The Anatolian Serotine appears to roost in colonies of 1-3 individuals. In Turkey , maternity colonies with 15-20 individuals and solitary individuals of both sexes, females occasionally having young, have been found. In Syria , Anatolian Serotines shared roosts with Savi’s Pipistrelles ( Hypsugo savii ), Greater Horseshoe Bats (Rhinolophus ferrumequinum), Lesser Myotis ( Myotis blythii ), Greater Myotis ( M. myotis ), and Natterer’s Myotis ( M. nattereri ). Status and Conservation. Not assessed on The IUCN Red List. The Anatolian Serotine is included under Botta’s Serotine, which is classified as Least Concern. Little is known regarding its ecology and threats, but it appears to be relatively widespread and is common around the eastern Mediterranean. Bibliography. Artyushin, Bannikova et al. (2009), Artyushin, Kruskop et al. (2018), Aulagnier et al. (2008), Benda, Abi-Said et al. (2016), Benda, Andreas et al. (2006), Benda, Hanék et al. (2007), Benda, Lucan et al. (2010), Dietz et al. (2007), Felten (1971), von Helversen (1998), Juste et al. (2013), Karatas & Sézen (2007), Mayeret al. (2007), Shehab et al. (2007), Volleth et al. (2001), Whitaker & Karatas (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	Eptesicus anatolicus	Eptesicus	Cnephaeus	anatolicus	Felten	1971	0	Senckenbergiana biol.	52(6): 371	Anatolian Serotine	None.		Greece and Cyprus through Turkey, S Lebanon, NW Syria, and W Iran.	Not listed.	Least Concern	Subgenus Cnephaeus . Distinct from bottae; see Han&aacute;k et al. (2001), Benda et al. (2006), Mayer et al. (2007), and Juste et al. (2012). May contain additional cryptic diversity see Juste et al. (2012).	Mammal Diversity Database. (2023). Mammal Diversity Database (Version 1.11) [Data set]. Zenodo. https://doi.org/10.5281/zenodo.7830771 released 15 April 2023	Eptesicus anatolicus	23	Anatolian Serotine	Anatolian Serotine Bat	Theria	Placentalia	Boreoeutheria	Laurasiatheria	CHIROPTERA	VESPERTILIONIFORMES	NA	NA	VESPERTILIONOIDEA	VESPERTILIONIDAE	VESPERTILIONINAE	EPTESICINI	Eptesicus	Cnephaeus	anatolicus	Felten	1971	0						Alanya, Antalya, Turkey.			anatolicus Felten, 1971	split from E. bottae	Juste, J., Benda, P., Garcia-Mudarra, J. L., & Ibanez, C. (2013). Phylogeny and systematics of Old World serotine bats (genus Eptesicus, Vespertilionidae, Chiroptera): an integrative approach. Zoologica Scripta, 42(5), 441-457.	Greece|Turkey|Cyprus|Syria|Lebanon|Iraq|Iran	Asia|Europe	Palearctic	LC	0	0	0	Eptesicus_anatolicus	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	Eptesicus anatolicus	ANIMALIA	CHORDATA	MAMMALIA	CHIROPTERA	VESPERTILIONIDAE	Eptesicus	anatolicus	Felten, 1971	In previous Red List assessments, Eptesicus anatolicus was included within E. bottae . It is now considered a separate species (Benda et al. 2006, Juste et al. 2013, Artyushin et al. 2018).	90000000	Eptesicus anatolicus	Least Concern		2021	2020-10-18 00:00:00 UTC	3.1	English	<p>Eptesicus anatolicus is assessed as Least Concern in view of its wide distribution, presumed large and stable population. If it is declining, it is unlikely to be declining fast enough to qualify for listing in a more threatened category.</p>	<p>Eptesicus anatolicus inhabits mostly Mediterranean shrubby habitats, avoiding mountains and forested areas in the West and more arid habitats in the East (e.g. Iran) (Benda et al. 2012, von Helversen 1998). Its roosting preferences are unknown, but one maternity roost has been found in Turkey in a building crevice, comprising 15 to 20 individuals. (Albayrak and Asan 1999). It is known to forage around streetlamps in Turkey and in the vicinity of urban areas on Rhodes (Benda et al. 2012, A. Lefebvre pers. comm.). It feeds on a range of insects. Orthoptera, Coleoptera, Odonata and Lepidoptera where the most common orders of insect preyed on in Iran whereas E. anatolicus seemed to feed almost exclusively on Carabidae (Coleoptera) in Turkey (Benda et al. 2012).</p>	Understanding of the threats to the species is limited as the ecology of the species is poorly known. This species, unlike E. bottae , seems to rely on Mediterranean habitats which are highly at risk because of climate change, mainly because of the increased occurrence of fires (Barredo et al. 2016) as well as urbanisation, especially in coastal areas (Cuttelod et al. 2009).	<p>This is a widespread, but relatively unknown species. It appears to be generally common, especially along the coast of South Anatolia as well as the Greek Islands. It appears to be quite rare in Lebanon from where there are very few records (Benda et al. 2016). The population is presumed to be stable.</p>	Stable	<p>This is a Middle eastern species distributed along a belt of Mediterranean habitats spanning from Rhodes and other Dodecanese Islands (Symi and Megisti) (Greece) to Iran (Spitzenberger 1994, von Helversen 1998, Hanak et al. 2001, Benda et al. 2016, Benda et al. 2018, Benda and Uhrin 2017, Mensoor 2020). The unique record in Northern Cyprus is believed to be an accidental record (Benda 2007, Benda 2018). It has been recorded from sea level to 1,310 m (Benda et al. 2012).</p> 		Terrestrial	This species is protected on the Greek Islands under the Bonn convention which needs to be updated to reflect taxonomic changes (NOTE: it is listed as Eptesicus bottae in said legislation). This species does not occur in protected areas. More research is needed to better understand the speciesâ€™ ecological needs and the dynamics of its populations in order to develop adequate conservation plans.	Palearctic		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	Eptesicus	Cnephaeus	anatolicus	Felten	1971	0	Senckenbergiana biol.	52(6): 371	Anatolian Serotine	None.		Greece and Cyprus through Turkey, S Lebanon, NW Syria, and W Iran.	Not listed.	Least Concern	Subgenus Cnephaeus . Distinct from bottae; see Han&aacute;k et al. (2001), Benda et al. (2006), Mayer et al. (2007), and Juste et al. (2012). May contain additional cryptic diversity see Juste et al. (2012).	Eptesicus anatolicus	1005511	23	Anatolian Serotine	Anatolian Serotine Bat	Theria	Placentalia	Boreoeutheria	Laurasiatheria	CHIROPTERA	VESPERTILIONIFORMES	NA	NA	VESPERTILIONOIDEA	Vespertilionidae	VESPERTILIONINAE	EPTESICINI	Eptesicus	Cnephaeus	anatolicus	Felten	1971	0						Alanya, Antalya, Turkey.			anatolicus Felten, 1971	split from E. bottae	Juste, J., Benda, P., Garcia-Mudarra, J. L., & Ibanez, C. (2013). Phylogeny and systematics of Old World serotine bats (genus Eptesicus, Vespertilionidae, Chiroptera): an integrative approach. Zoologica Scripta, 42(5), 441-457.				Greece|Turkey|Cyprus|Syria|Lebanon|Iraq|Iran	Asia|Europe	Palearctic	LC	0	0	0	Eptesicus_anatolicus	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	Cnephaeus_anatolicus	1005511	23	Anatolian Serotine	Anatolian Serotine Bat	Theria	Placentalia	Boreoeutheria	Laurasiatheria	Chiroptera	Yangochiroptera	NA	NA	Vespertilionoidea	Vespertilionidae	Vespertilioninae	Nycticeiini	Cnephaeus	NA	anatolicus	Felten	1	Eptesicus anatolicus	Felten, H. 1971-12-23. Eine neue Art der Fledermaus-Gattung _Eptesicus_ aus Kleinasien (Chiroptera: Vespertilionidae). Senckenbergiana biologica 52(6):371-376.		SMF:MAMM:36478	holotype		Alanya, Antalya, Turkey.			split from E. bottae; moved from Eptesicus to Cnephaeus	Juste, J., Benda, P., Garcia-Mudarra, J. L., & Ibanez, C. (2013). Phylogeny and systematics of Old World serotine bats (genus Eptesicus, Vespertilionidae, Chiroptera): an integrative approach. Zoologica Scripta, 42(5), 441-457.|ClÃ¡udio, V. C., Novaes, R. L., Gardner, A. L., Nogueira, M. R., Wilson, D. E., Maldonado, J. E., ... & Moratelli, R. (2023). Taxonomic re-evaluation of New World Eptesicus and Histiotus (Chiroptera: Vespertilionidae), with the description of a new genus. Zoologia (Curitiba), 40, e22029.				Greece|Turkey|Cyprus|Syria|Lebanon|Iraq|Iran	Asia|Europe	Palearctic	LC (as Eptesicus anatolicus)	0	0	0	Eptesicus_anatolicus	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	Cnephaeus		anatolicus	Felten	1971	1	Senckenbergiana biol.	52(6): 371	Anatolian Serotine	None.	Turkey, Antalya, Alanya	Greece and Cyprus through Turkey, S Lebanon, NW Syria, and W Iran.	<a href='https://cites.org/eng/app/appendices.php' target='_blank'>Not Listed</a>	<a href='https://www.iucnredlist.org/species/85198368/85199537/' target='_blank'>Least Concern as Eptesicus anatolicus</a>	Distinct from bottae; see Han&aacute;k et al. (2001), Benda et al. (2006), Mayer et al. (2007), and Juste et al. (2012). May contain additional cryptic diversity see Juste et al. (2012).		Mammal Diversity Database. (2025). Mammal Diversity Database (Version 2.2) [Data set]. Zenodo. https://doi.org/10.5281/zenodo.15007505	NA	Eptesicus anatolicus; Eptesicus anatolicus; Eptesicus anatolicus; Eptesicus anatolicus; Eptesicus anatolicus; anatolicus; Sérotine d'Anatolie; Anatolien-Breitflligelfledermaus; Eptesicus de Anatolia; Anatolian Serotine Bat; Anatolian Serotine; Anatolian Serotine Bat; Anatolian Serotine; E. anatolicus
