Over a thousand years of evolutionary history of domestic geese from Russian archaeological sites, analysed using ancient DNA

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Supplementary information for: Over a thousand years of evolutionary history of domestic geese from Russian archaeological sites, analysed using ancient DNA Johanna Honka, Matti T. Heino, Laura Kvist, Igor V. Askeyev, Dilyara N. Shaymuratova, Oleg V. Askeyev, Arthur O. Askeyev, Marja E. Heikkinen, Jeremy B. Searle and Jouni Aspi Table S1. List of the successfully sequenced subfossil goose samples (n = 51) from Russia with their haplotype and species inferred from the concatenated hypervariable part of the mtdna (mitochondrial DNA) control region sequences (204 bp). The haplotype names follow the nomenclature in [1] for domestic and greylag goose (Anser anser) and [2] for taiga bean goose (A. fabalis fabalis). Forward slashes between haplotype names denote haplotypes that differ over the whole control region sequence (1249 bp [1]) but cannot be distinguished in the 204 bp sequence analysed here. In addition, the archaeological information is listed with the species inferred from bone morphology, the studied skeletal element, the sample dating by the archaeological context, the assigned temporal period of the samples, the excavation site and the location of site. Sample name Haplotype Species based on mtdna Species based on bone morphology Studied bone fragment Archaeological dating Time period Archaeological site Location of site JH24 Fa5 Taiga bean goose ulna/humerus 4 th -8 th Early Medieval Tetyushskoe II hillfort JH25 Fa5 Taiga bean goose humerus JH1 JH23 F11 F11 tibiotarsus furcula JH39 FAB1 Taiga bean goose tibiotarsus JH40 Fa3 Taiga bean goose femur JH37 F6 JH38 D3/D7 humerus tarsometatarsus 4 th -8 th 4 th -8 th 5 th -7 th 9 th - 10 th 9 th - 10 th 11 th -12 th 11 th -12 th Early Medieval Early Medieval Tetyushskoe II hillfort Tetyushskoe II hillfort Early Medieval Imenkov hillfort Early Medieval Staraya Ladoga Leningrad Region Early Medieval Staraya Ladoga Leningrad Region Ostolopovskoe settlement Ostolopovskoe settlement

JH29 Fa6 Taiga bean goose femur JH30 D3/D7 humerus JH31 D3/D7 tibiotarsus JH56 ulna JH28 sternum JH47 D3/D7 JH48 D3/D7 JH49 JH50 JH51 F6 JH52 Fa3 Taiga bean goose JH53 humerus tibiotarsus tarsometatarsus tibiotarsus tibiotarsus ulna / tarsometatarsus 11 th -13 th 12 th -13 th 12 th -13 th 12 th -13 th Bilyarsk (Defensive moat locationperipherals of settlement) Bilyarsk (Palace lord location - downtown) Bilyarsk (Palace lord location - downtown) Elabuga hillfort Bagaevskoe settlement Kremlin Kremlin Kremlin Saratov Region Region Region Region Bulgar Bulgar Bulgar Bulgar JH32 D3/D7 humerus 15 th century CE Late Medieval Toretskoe settlement JH33 D3/D7 humerus 15 th century CE Late Medieval Toretskoe settlement JH34 D3/D7 humerus 15 th century CE Late Medieval Toretskoe settlement JH35 F6 humerus 15 th century CE Late Medieval Toretskoe settlement

JH16 radius JH17 humerus JH18 humerus JH2 humerus JH3 humerus JH4 humerus JH5 humerus JH6 D3/D7 coracoideum JH7 coracoideum JH8 D3/D7 coracoideum JH10 D3/D7 femur JH11 femur JH12 tibiotarsus

JH13 tarsometatarsus JH14 carpometacarpus JH61 D3/D7 femur 16 th -18 th Cheboksary city Chuvash Republic JH62 D3/D7 humerus 16 th -18 th Cheboksary city Chuvash Republic JH64 D3/D7 tibiotarsus 16 th -18 th Cheboksary city Chuvash Republic JH45 tibiotarsus first half of 16 th century CE Pskov city (New Torg location) Pskov Region JH46 tibiotarsus first half of 16 th century CE Pskov city (New Torg location) Pskov Region JH54 D3/D7 humerus 17 th 18 th Elabuga hillfort JH55 D3/D7 tibiotarsus 17 th 18 th Elabuga hillfort JH65 humerus 17 th century CE Sviyazhsk JH66 tibiotarsus 17 th century CE Sviyazhsk JH58 F6 furcula 18 th century CE Late Post-Medieval Kazan Kremlin JH59 humerus 18 th century CE Late Post-Medieval Kazan Kremlin JH60 humerus 18 th century CE Late Post-Medieval Kazan Kremlin

Table S2. Variable nucleotide sites in the concatenated 204 base pairs of the mitochondrial control region haplotypes discovered among ancient domestic goose samples from Russian archaeological sites. Haplotypes FAB1, Fa3, Fa5 and Fa6 belong to another species, the taiga bean goose (Anser fabalis fabalis), but were discovered among the morphologically identified domestic/wild greylag goose subfossil bones. Position Haplotype 2 5 13 14 19 25 26 35 38 41 44 71 86 89 91 92 97 102 103 109 113 118 121 135 142 155 168 169 172 178 T A G C C G A C A G A C A T T A A C T C T C A G T T C T C T D3/D7.... T......................... F6... T T... G A.. G C........... C... C F11... T T... G A.. G C........... C. C.. FAB1 A G A T T A G T.. G T.. C G G T C T C T C A C. T C T C Fa3 A G A T T A G T.. G T.. C G G T C T C T C A C. T. T C Fa5 A G A T T A G T.. G T.. C. G T C T C T C A C. T C T C Fa6 A. A T T A G T.. G T.. C G G T C T C T C A C. T. T C

Text S1. Archaeological and historical context of the samples 1. Archaeological record Based on bird bones from archaeological sites from the European part of Russia and Ukraine, it can be concluded that the first authentic appearance and existence of domestic geese in this area occurred in the 6 th century BCE - 4 th century CE in the northern Black Sea region [3-6]. In this area, ancient Greek city-colonies (Olbia, Phanagoria, Tanais, etc.) and states such as the Bosporan kingdom existed [7]. The archaeological remains of domestic goose can be found in many Medieval settlements, both urban and rural, in Ukraine, Belarus and the European part of Russia, with the exception of the northern regions [4-6,8-13]. In western Siberia, the domestic goose appeared at the end of the 16 th century and at the beginning of the 17 th century as a result of the Russian colonisation of Siberia and the establishment of large trade settlements [14-15]. 2. Historical context 2.1. Local goose breeds in the vicinity of the In some remote villages inhabited by Udmurts and Maris up to the 1970s, the breeding of strictly local geese took place, which had the appearance and behavioural characteristics of greylag geese (Anser anser) [16]. These geese flew very well, had very good parenting skills, laid eggs and incubated them without human help, the colour of feathers and the body size was the same as that of wild geese and these geese also made flights far from home [16]. But over the past 50 years, apparently, the practice of breeding these geese has not survived. In the Urals, at the end of the 17 th century, the Shadrin breed was established on the basis of interbreeding of local wild geese and a local breed of domestic goose [17]. This breed did not experience the inflow of genes from other breeds of geese. Only small numbers of this breed currently survive [17]. A very interesting breed of geese was created in the 19 th century in the Pskov Region, called the Pskov bald goose [17]. It was obtained as a result of crossing local domestic geese with wild greater white-fronted geese (A. albifrons). The average goose has a horizontal body, red-orange legs and bill, a blue or light-grey plumage with a white spot on the forehead [17]. 2.2. Practices of egg and gosling collection Extensive data exist in the historical and ornithological literature about collecting goose eggs and catching goslings for their further rearing in captivity in Ukraine, Russia and Kazakhstan. In the middle of the 16 th century, Miehalonis Litnani [18] reported on the practice of collecting wild goose eggs to obtain goslings for captive rearing in the Dnieper Region of Ukraine. P.I. Rychkov [19] describes that in the middle of the 18 th century, the inhabitants of the new fortresses in Orenburg Province caught goslings of the greylag goose, and raised them together with domestic geese. In the Urals, at the end of the 19 th century and the first third of the 20 th century, the Bashkirs practised collection of wild greylag goose eggs and putting them under domestic geese in order to produce goslings [20]. Rearing of goslings of grey geese caught from the wild was also practised in the first third of the 20 th century in several regions of Kazakhstan [21,22]. The most widespread captive breeding of the wild greylag geese from eggs and catching of small goslings took place in the south of western Siberia, particularly in the Barabinsk Area (steppe) [22,23]. Quite recently, in the 1950s and 1970s, in the north of the Arkhangelsk Region and in the west of the Komi Republic, the local people practised catching goslings of the taiga bean goose (A. fabalis) for captive breeding [24,25]. Ornithologists and naturalists of the 19 th and early 20 th centuries noted that the locals of the Baikal and Amur Regions caught goslings of swan goose (A. cygnoid) for captivity, in which they were quickly tamed and kept until autumn [26,27]. 2.3. Bean geese in the According to ornithological studies in the 19 th and 20 th centuries in the Middle Volga Region, the bean goose was a numerous migrating goose [28-33]. The numbers of various bean goose taxa varied considerably

between years in the Middle Volga Region at the end of the 19 th century and the first third of the 20 th century. So in the early 1890s, the tundra bean goose (Melanonyx segetum = A. fabalis rossicus) predominated to a considerable extent, with the main range spanning between Kazan and the Kama River and along the valley of this river. The taiga bean goose (Melanonyx arvensis = A. fabalis fabalis) occurred in small numbers with the main migration route following the Volga River [30]. By the late 1920s and early 1930s, in the same area, migratory flocks of the taiga bean goose (M. arvensis = A. f. fabalis) prevailed, and the numbers of the tundra bean goose (M. segetum = A. f. rossicus) were significantly smaller [31]. Monitoring of the spring migration (April-May) of the bean goose in the (2016-2017) showed that the tundra bean goose (A. f. rossicus) predominated in the years 2016 (94.5 %) and 2017 (93.4 %) with taiga bean goose (A. f. fabalis) constituting 5.5 % and 6.6 %, respectively [34]. The taiga bean goose has a flyway along the valley of the Volga River to Kazan, and then along the valleys of the Ashit, Kazanka and Miesha Rivers and to the Vyatka River and along its valley northwards. The main flyway of the tundra bean goose goes from south of Kazan to the Kama River, and then along its valley eastwards and northeastwards. Fifteen bean geese obtained during the spring hunt in 2015-2017 from different parts of the were also examined and morphologically identified. Of these, tundra bean goose comprised 14 specimens (93.3 %) and one specimen (6.7 %) was the typical taiga bean goose. Thus, both the taiga and the tundra bean goose migrate across the Middle Volga Region and have done so in the past. References 1. Heikkinen, M.E.; Ruokonen, M.; Alexander, M.; Aspi, J.; Pyhäjärvi, T.; Searle, J.B. Relationship between wild greylag and European domestic geese based on mitochondrial DNA. Anim. Genet. 2015, 46, 485-497. 2. Honka, J.; Kvist, L.; Heikkinen, M.E.; Helle, P.; Searle, J.B.; Aspi, J. Determining the subspecies composition of bean goose harvests in Finland using genetic methods. Eur. J. Wildl. Res. 2017, 63, 19. 3. Voinstvensky, M.A. Ornithofauna of Olbia. Archaeological Sites of Ukraine. No 7 (in Ukrainian); Institute of Archeology: Kiev, Ukraine, 1958. 4. Voinstvensky, M.A. Fossil Avifauna of Ukraine (in Russian); The Natural Environment and the Fauna of the Past: Kiev, Ukraine, 1967. 5. Burchak-Abramovich, N.I.; Tsalkin, V.I. To the knowledge of the avifauna of South Ukraine, Crimea and the Don Region (according to archaeological materials) (in Russian). Bulletin of the Moscow Society of Naturalists (Biological series) 1971, 76, 54-63. 6. Umanskaya, A.S. Domestic Birds from Archaeological Sites of Ukraine (in Russian); Natural Environment and Fauna of the Past: Kiev, Ukraine, 1972. 7. Koshelenko, G.A.; Kruglikova, I.T.; Dolgorukov, V.S., Eds. Ancient States of the Northern Black Sea Littoral (in Russian); Archeology of the USSR, Nauka: Moscow, Russia, 1984. 8. Burchak-Abramovich, N.I.; Tsalkin, V.I. Birds from archaeological excavations in the Moscow Kremlin (in Russian). Bulletin of the Moscow Society of Naturalists (Biological series) 1969, 74, 49-53. 9. Burchak-Abramovich, N.I.; Tsalkin, V.I. Materials for the study of European birds of RSFSR (according to archaeological sites) (in Russian). Bulletin of the Moscow Society of Naturalists (Biological series) 1972, 77, 51-59. 10. Bryuzgina (Umanskaya), A.S. Late Anthropogenic Birds from the Ukraine and Contiguous Territories (Primarily Based on Materials from Archeological Sites) (in Russian). Thesis for a Candidate of Biological Science, Institute of Zoology, Kiev, 1975. 11. Askeyev, I.V.; Galimova, D.N.; Askeyev, O.V. Birds of the Middle Volga Region during the V XVIII centuries AD (according to archaeological excavations) (in Russian). Volga River Region Archaeology (Zhurnal Povolzskaya Arkheologiya) 2013, 3, 116-144. 12. Galimova, D.N.; Askeyev, I.V.; Askeyev, O.V. Bird remains from 5th - 17th century AD archaeological sites in the Middle Volga region of Russia. Int. J. Osteoarchaeol. 2014, 24, 347-357. 13. Gorobets, L.; Kovalchuk, O. Birds in the medieval culture and economy of the East Slavs in the 10-13th centuries AD. Environ. Archeol. 2017, 22, 147-165. 14. Nekrasov, A.E. Bone Remains of Birds from the Holocene Locations of the Urals and Western Siberia (in Russian); Quaternary paleozoology in the Urals: Yekaterinburg, Russia 2003. 15. Martynovich, N.V. Birds of "Gold-Fired" Mangazeya (in Russian). Zoological Journal 2013, 92, 1129-1135.

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