Palaeogenomic analysis of black rat (Rattus rattus) reveals multiple European introductions associated with human economic history

. 2022 May 03 ; 13 (1) : 2399. [epub] 20220503

Jazyk angličtina Země Velká Británie, Anglie Médium electronic

Typ dokumentu časopisecké články, Research Support, U.S. Gov't, Non-P.H.S., práce podpořená grantem

Perzistentní odkaz   https://www.medvik.cz/link/pmid35504912

Grantová podpora
209817/Z Wellcome Trust - United Kingdom

Odkazy

PubMed 35504912
PubMed Central PMC9064997
DOI 10.1038/s41467-022-30009-z
PII: 10.1038/s41467-022-30009-z
Knihovny.cz E-zdroje

The distribution of the black rat (Rattus rattus) has been heavily influenced by its association with humans. The dispersal history of this non-native commensal rodent across Europe, however, remains poorly understood, and different introductions may have occurred during the Roman and medieval periods. Here, in order to reconstruct the population history of European black rats, we first generate a de novo genome assembly of the black rat. We then sequence 67 ancient and three modern black rat mitogenomes, and 36 ancient and three modern nuclear genomes from archaeological sites spanning the 1st-17th centuries CE in Europe and North Africa. Analyses of our newly reported sequences, together with published mitochondrial DNA sequences, confirm that black rats were introduced into the Mediterranean and Europe from Southwest Asia. Genomic analyses of the ancient rats reveal a population turnover in temperate Europe between the 6th and 10th centuries CE, coincident with an archaeologically attested decline in the black rat population. The near disappearance and re-emergence of black rats in Europe may have been the result of the breakdown of the Roman Empire, the First Plague Pandemic, and/or post-Roman climatic cooling.

ArchaeoBone Blekenweg 61 9753 JN Haren The Netherlands

Archaeological Services University of Durham Durham UK

Archaeology of Social Dynamics IMF CSIC Barcelona 08001 Spain

Archaeozoology Archaeobotany Societies Practices Environments Paris France

Archeoplan Eco 2616 LZ Delft Netherlands

Austrian Academy of Sciences Austrian Archaeological Institute Hollandstraße 11 13 1020 Vienna Austria

BioArCh Department of Archaeology University of York York YO1 7EP UK

Canterbury Archaeological Trust 92a Broad Street Canterbury Kent CT1 2LU UK

Centre for Palaeogenetics and Department of Geological Sciences Stockholm University Stockholm 10691 Sweden

Centre National de la Recherche Scientifique University of Lille Lille France

Centro de Arqueologia da Universidade de Lisboa Faculdade de Letras Universidade de Lisboa 1600 214 Lisboa Portugal

Charité Universitätsmedizin Berlin Institut für Pathologie Charitéplatz 1 10117 Berlin Germany

Christian Archaeology and Byzantine Art History Philipps University of Marburg 35037 Marburg Germany

Consell Insular d'Eivissa i Formentera Avenida de España 49 07800 Eivissa Illes Balears Spain

Cultural Heritage Agency of the Netherlands Smallepad 5 3811 MG Amersfoort The Netherlands

Department of Anthropology Rice University 6100 Main St Houston TX 77005 USA

Department of Anthropology University of British Columbia Vancouver BC Canada

Department of Anthropology University of California Santa Cruz 1156 High St Santa Cruz CA 95064 USA

Department of Archaeogenetics Max Planck Institute for Evolutionary Anthropology 04103 Leipzig Germany

Department of Archaeogenetics Max Planck Institute for the Science of Human History 07745 Jena Germany

Department of Archaeology and Anthropology Bournemouth University Poole BH12 5BB UK

Department of Archaeology Classics and Egyptology University of Liverpool Liverpool L69 7WZ UK

Department of Archaeology Durham University Durham UK

Department of Archaeology Institute of History and Archaeology University of Tartu 2 Jakobi St 51005 Tartu Estonia

Department of Archaeology Max Planck Institute for the Science of Human History 07745 Jena Germany

Department of Archaeology Simon Fraser University Burnaby BC V5 1S6 Canada

Department of Archaeology Sir Marcus Fernando Mawatha Colombo 07 Sri Lanka

Department of Archaeology University of Aberdeen Aberdeen AB24 3UF UK

Department of Archaeology University of Reading Berkshire RG6 6AB UK

Department of Archaeology University of Sydney Sydney NSW 2006 Australia

Department of Archaeology University of York York YO1 7EP UK

Department of Culture University of Helsinki P O Box 59 FI 00014 Helsinki Finland

Department of Ecology and Evolutionary Biology Cornell University Ithaca NY 14853 USA

Department of History and Archaeology University of Ruhuna Matara 81000 Sri Lanka

Department of Natural Sciences and Archaeometry Institute of Archaeology of the Czech Academy of Sciences Prague Letenská 4 118 01 Prague Czech Republic

Department of Philosophy Institute of Prehistoric Archaeology Friedrich Alexander University of Erlangen Nürnberg 91054 Erlangen Germany

Departmento de Biología Universidad Autónoma de Madrid 28049 Madrid Spain

Fell View Park Gosforth Seascale Cumbria CA20 1HY UK

Freelance archaeozoologist Liliom u 4 1 1 Balatonfüred 8230 Hungary

Institut National de Patrimoine Tunis 1008 Tunisia

Institute of Archaeology 11000 Belgrade Serbia

Institute of Archaeology University College London London WC1H 0PY UK

Institute of Clinical Molecular Biology Kiel University Kiel 24105 Germany

L'Ecole Tunisienne de l'Histoire et l'Anthropologie Tunis Tunisia

Laboratory of Biodiversity and Evolutionary Genomics Katholieke Universiteit Leuven 3000 Leuven Belgium

Museum of Vertebrate Zoology University of California Berkeley Berkeley CA 94720 3160 USA

Negaunee Integrative Research Center Field Museum of Natural History Chicago IL 60605 USA

Osteological Research Laboratory University of Stockholm 10691 Stockholm Sweden

Palaeogenomics and Bio Archaeology Research Network Research Laboratory for Archaeology and History of Art University of Oxford Oxford OX1 3QY UK

Postgraduate Institute of Archaeology 407 Bauddhaloka Mawatha Colombo 7 Sri Lanka

Research Centre in Evolutionary Anthropology and Palaeoecology Liverpool John Moores University Liverpool L3 3AF UK

Römisch Germanisches Zentralmuseum Leibniz Forschungsinstitut für Archäologie Ernst Ludwig Platz 2 55116 Mainz Germany

Royal Belgian Institute of Natural Sciences Vautierstraat 29 1000 Brussels Belgium

Schmalhausen Institute of Zoology National Academy of Sciences of Ukraine Kyiv 01030 Ukraine

School of Life Sciences Peking University 100871 Beijing China

School of Social Science The University of Queensland St Lucia QLD Australia

Secció de Prehistòria i Arqueologia University of Barcelona Barcelona Spain

Ukrainian Scientific Center of Ecology of the Sea Odessa 65009 Ukraine

University of Tunis Tunis Tunisia

VIAS Vienna Institute for Archaeological Science University of Vienna Althanstraße 14 1090 Vienna Austria

Zobrazit více v PubMed

Boivin NL, et al. Ecological consequences of human niche construction: Examining long-term anthropogenic shaping of global species distributions. Proc. Natl Acad. Sci. USA. 2016;113:6388–6396. doi: 10.1073/pnas.1525200113. PubMed DOI PMC

Capizzi D, Bertolino S, Mortelliti A. Rating the rat: global patterns and research priorities in impacts and management of rodent pests. Mamm. Rev. 2014;44:148–162. doi: 10.1111/mam.12019. DOI

Meerburg BG, Singleton GR, Kijlstra A. Rodent-borne diseases and their risks for public health. Crit. Rev. Microbiol. 2009;35:221–270. doi: 10.1080/10408410902989837. PubMed DOI

McCormick M. Rats, communications, and plague: toward an ecological history. J. Interdiscip. Hist. 2003;34:1–25. doi: 10.1162/002219503322645439. DOI

Aplin, K. P., Brown, P., Jacob, J., Krebs, C. J. & Singleton, G. R. Field Methods for Rodent Studies in Asia and the Indo-Pacific (Australian Centre for International Agricultural Research, 2003).

Lack JB, et al. Invasion facilitates hybridization with introgression in the Rattus rattus species complex. Mol. Ecol. 2012;21:3545–3561. doi: 10.1111/j.1365-294X.2012.05620.x. PubMed DOI

Conroy CJ, et al. Cryptic genetic diversity in Rattus of the San Francisco Bay region, California. Biol. Invasions. 2013;15:741–758. doi: 10.1007/s10530-012-0323-9. DOI

Robins JH, Hingston M, Matisoo-Smith E, Ross HA. Identifying Rattus species using mitochondrial DNA. Mol. Ecol. Notes. 2007;7:717–729. doi: 10.1111/j.1471-8286.2007.01752.x. DOI

Pagès M, et al. Revisiting the taxonomy of the Rattini tribe: a phylogeny-based delimitation of species boundaries. BMC Evol. Biol. 2010;10:184. doi: 10.1186/1471-2148-10-184. PubMed DOI PMC

Aplin KP, et al. Multiple geographic origins of commensalism and complex dispersal history of Black Rats. PLoS ONE. 2011;6:e26357. doi: 10.1371/journal.pone.0026357. PubMed DOI PMC

Robins JH, et al. Dating of divergences within the Rattus genus phylogeny using whole mitochondrial genomes. Mol. Phylogenet. Evol. 2008;49:460–466. doi: 10.1016/j.ympev.2008.08.001. PubMed DOI

Yosida TH, Kato H, Tsuchiya K, Moriwaki K. Karyotypes and serum transferrin patterns of hybrids between Asian and Oceanian black rats, Rattus rattus. Chromosoma. 1971;34:40–50. doi: 10.1007/BF00285515. PubMed DOI

Hulme-Beaman A, Dobney K, Cucchi T, Searle JB. An ecological and evolutionary framework for commensalism in anthropogenic environments. Trends Ecol. Evol. 2016;31:633–645. doi: 10.1016/j.tree.2016.05.001. PubMed DOI

Jones EP, Eager HM, Gabriel SI, Jóhannesdóttir F, Searle JB. Genetic tracking of mice and other bioproxies to infer human history. Trends Genet. 2013;29:298–308. doi: 10.1016/j.tig.2012.11.011. PubMed DOI

Puckett EE, Orton D, Munshi-South J. Commensal rats and humans: integrating rodent phylogeography and zooarchaeology to highlight connections between human societies. Bioessays. 2020;42:e1900160. doi: 10.1002/bies.201900160. PubMed DOI

Jones EP, et al. Fellow travellers: a concordance of colonization patterns between mice and men in the North Atlantic region. BMC Evol. Biol. 2012;12:35. doi: 10.1186/1471-2148-12-35. PubMed DOI PMC

Cucchi T. Uluburun shipwreck stowaway house mouse: molar shape analysis and indirect clues about the vessel’s last journey. J. Archaeol. Sci. 2008;35:2953–2959. doi: 10.1016/j.jas.2008.06.016. DOI

Cucchi T, et al. On the trail of Neolithic mice and men towards Transcaucasia: zooarchaeological clues from Nakhchivan (Azerbaijan) Biol. J. Linn. Soc. Lond. 2013;108:917–928. doi: 10.1111/bij.12004. DOI

Cucchi T, et al. Tracking the Near Eastern origins and European dispersal of the western house mouse. Sci. Rep. 2020;10:8276. doi: 10.1038/s41598-020-64939-9. PubMed DOI PMC

Matisoo-Smith E, Robins JH. Origins and dispersals of Pacific peoples: evidence from mtDNA phylogenies of the Pacific rat. Proc. Natl Acad. Sci. USA. 2004;101:9167–9172. doi: 10.1073/pnas.0403120101. PubMed DOI PMC

Matisoo-Smith E, Robins J. Mitochondrial DNA evidence for the spread of Pacific rats through Oceania. Biol. Invasions. 2009;11:1521–1527. doi: 10.1007/s10530-008-9404-1. DOI

West K, et al. The Pacific Rat Race to Easter Island: tracking the prehistoric dispersal of Rattus exulans using ancient mitochondrial genomes. Front. Ecol. Evol. 2017;5:52. doi: 10.3389/fevo.2017.00052. DOI

Niethammer VJ. Zur Taxonomie und Ausbreitungsgeschichte der Hausratte (Rattus rattus) Zool. Anz. Jena. 1975;194:405–415.

Baig M, Khan S, Eager H, Atkulwar A, Searle JB. Phylogeography of the black rat Rattus rattus in India and the implications for its dispersal history in Eurasia. Biol. Invasions. 2019;21:417–433. doi: 10.1007/s10530-018-1830-0. DOI

Tchernov E. Commensal animals and human sedentism in the Middle East. Anim. Archaeol. 1984;3:91–115.

Ervynck, A. Sedentism or urbanism? On the origin of the commensal black rat (Rattus rattus). In Bones and the Man: Studies in Honour of Don Brothwell (eds Dobney, K. & O’Connor, T. P.) 95–109 (Oxbow, 2002).

Ruffino L, Vidal E. Early colonization of Mediterranean islands by Rattus rattus: a review of zooarcheological data. Biol. Invasions. 2010;12:2389–2394. doi: 10.1007/s10530-009-9681-3. DOI

Vigne J-D, Valladas HÈ. Small mammal fossil assemblages as indicators of environmental change in Northern Corsica during the last 2500 years. J. Archaeol. Sci. 1996;23:199–215. doi: 10.1006/jasc.1996.0018. DOI

Oueslati T, et al. 1st century BCE occurrence of chicken, house mouse and black rat in Morocco: socio-economic changes around the reign of Juba II on the site of Rirha. J. Archaeol. Sci.: Rep. 2020;29:102162.

Audoin-Rouzeau F, Vigne J-D. La colonisation de l’Europe par le rat noir (Rattus rattus) Rev. Paléobiol. 1994;13:125–145.

Audoin-Rouzeau F, Vigne ETJ-D. Le rat noir (Rattus rattus) en Europe Antique et mediévale: les voies du commerce et l’expansion de la peste. Anthropozoologica. 1997;25/26:399–404.

Armitage PL. Unwelcome companions: ancient rats reviewed. Antiquity. 1994;68:231–240. doi: 10.1017/S0003598X00046548. DOI

Hufthammer AK, Walløe L. Rats cannot have been intermediate hosts for Yersinia pestis during medieval plague epidemics in Northern Europe. J. Archaeol. Sci. 2013;40:1752–1759. doi: 10.1016/j.jas.2012.12.007. DOI

Dean KR, et al. Human ectoparasites and the spread of plague in Europe during the Second Pandemic. Proc. Natl Acad. Sci. USA. 2018;115:1304–1309. doi: 10.1073/pnas.1715640115. PubMed DOI PMC

Sloane, B. The Black Death in London (The History Press, 2011).

Hardy A. The under-appreciated rodent: harbingers of plague from the middle ages to the twenty-first century. J. Interdiscip. Hist. 2019;50:171–185. doi: 10.1162/jinh_a_01408. DOI

White LA, Mordechai L. Modeling the Justinianic Plague: comparing hypothesized transmission routes. PLoS One. 2020;15:e0231256. doi: 10.1371/journal.pone.0231256. PubMed DOI PMC

O’Connor TP. On the lack of bones of the ship rat Rattus rattus from Dark Age York. J. Zool. 1991;224:318–320. doi: 10.1111/j.1469-7998.1991.tb04809.x. DOI

Rielly, K. The black rat. In Extinctions and Invasions: a Social History of British fauna (eds O’Connor, T. & Sykes, N.) 134–145 (Oxbow, 2010).

Salvadori, F. The transition from late antiquity to early Middle Ages in Italy. A zooarchaeological perspective. Quat. Int. 10.1016/j.quaint.2018.06.040 (2018).

De Cupere B, et al. Eagle owl (Bubo bubo) pellets from Roman Sagalassos (SW Turkey): distinguishing the prey remains from nest and roost sites. Int. J. Osteoarchaeol. 2009;19:1–22. doi: 10.1002/oa.965. DOI

Parfitt, S. A. The small mammals. In The Transition To Late Antiquity on the Danube and Beyond (ed. Poulter, A. G.) 198–318 (Oxford University Press, 2007).

Davis, E. M. Paleoecological studies at Stobi. In Studies in the Antiquities of Stobi, Vol. 3 (eds Aleksova, B., Wiseman, J. & Mano-Zisi, Đ.) (Princetion University Press, 1981).

Baron H, Reuter AE, Marković N. Rethinking ruralization in terms of resilience: subsistence strategies in sixth-century Caričin Grad in the light of plant and animal bone finds. Quat. Int. 2019;499:112–128. doi: 10.1016/j.quaint.2018.02.031. DOI

Benedictow, O. J. What Disease was Plague?: On the Controversy Over the Microbiological Identity of Plague Epidemics of the Past (Brill, 2010).

O’Connor, T. P. Bones from Anglo-Scandinavian levels at 16–22 Coppergate. (Council for British Archaeology, 1989).

Pasda, K. Tierknochen als Spiegel sozialer Verhältnisse im 8.-15. Jh. in Bayern (Praehistoricaverlag, 2004).

Dobney, K., Jacques, D., Barrett, J. & Johnstone, C. Farmers, Monks and Aristocrats: the Environmental Archaeology of Anglo-Saxon Flixborough (Oxbow, 2007).

Reichstein, H. Die wildlebenden Säugetiere von Haithabu: Ausgrabungen 1966–1969 und 1979–1980. (Karl Wachholtz, 1991).

Wigh, B. Animal husbandry in the Viking Age town of Birka and its hinterland: excavations in the black earth 1990–95 (Riksantikvarieämbetet, 2001).

Tourunen, A. Animals in an Urban Context—A Zooarchaeological Study of the Medieval and Post-Medieval town of Turku (University of Turku, 2008).

Ervynck, A. Archeozoölogisch onderzoek van de zwarte rat (Rattus rattus) en de bruine rat (Rattus norvegicus) (Doctoral thesis, Amsterdam, 1989).

Barrett-Hamilton, G. & Hinton, M. A History of British Mammals (Gurney and Jackson, 1910).

Mitchell-Jones, A. J. et al. The Atlas of European Mammals (Poyser, 1999).

Savinetsky AB, Krylovich OA. On the history of the spread of the black rat (Rattus rattus L., 1758) in northwestern Russia. Biol. Bull. Russ. Acad. Sci. 2011;38:203–207. doi: 10.1134/S1062359011020130. PubMed DOI

Ward-Perkins, B. The Fall of Rome and the End of Civilization (Oxford University Press, 2005).

Wickham, C. Framing the Early Middle Ages: Europe and the Mediterranean 400–800 (Oxford University Press, 2005).

Horden, P. & Purcell, N. The Corrupting Sea: A Study of Mediterranean History (Wiley-Blackwell, 2000).

Ambrosiani, B. Osten und Westen im Ostseehandel zur Wikingerzeit. In Haithabu und die frühe Stadtentwicklung im nördlichen Europa (eds Brandt, K., Müller-Wille, M. & Radtke, C.) 339–348 (Wachholtz, 2002).

Hodges, R. Dark Age Economics: A New Audit (Bloomsbury, 2012).

Keller M, et al. Ancient Yersinia pestis genomes from across Western Europe reveal early diversification during the First Pandemic (541–750) Proc. Natl Acad. Sci. USA. 2019;116:12363–12372. doi: 10.1073/pnas.1820447116. PubMed DOI PMC

Wagner DM, et al. Yersinia pestis and the Plague of Justinian 541–543 AD: a genomic analysis. Lancet Infect. Dis. 2014;14:319–326. doi: 10.1016/S1473-3099(13)70323-2. PubMed DOI

Feldman M, et al. A high-coverage Yersinia pestis genome from a sixth-Century Justinianic Plague victim. Mol. Biol. Evol. 2016;33:2911–2923. doi: 10.1093/molbev/msw170. PubMed DOI PMC

Putnam NH, et al. Chromosome-scale shotgun assembly using an in vitro method for long-range linkage. Genome Res. 2016;26:342–350. doi: 10.1101/gr.193474.115. PubMed DOI PMC

Simão FA, Waterhouse RM, Ioannidis P, Kriventseva EV, Zdobnov EM. BUSCO: assessing genome assembly and annotation completeness with single-copy orthologs. Bioinformatics. 2015;31:3210–3212. doi: 10.1093/bioinformatics/btv351. PubMed DOI

Li H, Durbin R. Inference of human population history from individual whole-genome sequences. Nature. 2011;475:493–496. doi: 10.1038/nature10231. PubMed DOI PMC

Deinum EE, et al. Recent evolution in Rattus norvegicus is shaped by declining effective population size. Mol. Biol. Evol. 2015;32:2547–2558. doi: 10.1093/molbev/msv126. PubMed DOI PMC

Gronau I, Hubisz MJ, Gulko B, Danko CG, Siepel A. Bayesian inference of ancient human demography from individual genome sequences. Nat. Genet. 2011;43:1031–1034. doi: 10.1038/ng.937. PubMed DOI PMC

Colangelo P, et al. Mitochondrial phylogeography of the black rat supports a single invasion of the western Mediterranean basin. Biol. Invasions. 2015;17:1859–1868. doi: 10.1007/s10530-015-0842-2. DOI

Etougbétché J, et al. Genetic diversity and origins of invasive black rats (Rattus rattus) in Benin, West Africa. fozo 1. 2020;69:20014.1.

Hemamali PPC, Boyagoda SH. Historic black rat invasions into Sri Lanka lead to hybridization forming two sub-lineages in the Rattus rattus species complex. Ceylon J. Sci. 2020;49:433. doi: 10.4038/cjs.v49i4.7823. DOI

Carleton, G. G., Musserand, M. D. & Musser, G. G. Superfamily Muroidea. In Mammal Species of the World: A Taxonomic and Geographic Reference 3rd edn (eds Wilson, D. E. & Reeder, D. M.) 894–1531 (Johns Hopkins University Press, 2005).

Boivin, N. Proto-globalisation and biotic exchange in the old world. In Human Dispersal and Species Movement from Prehistory to the Present (eds Boivin, N., Crassard, R. & Petraglia, M.) 349–408 (Cambridge University Press, 2017).

Cooper, J. P. Egypt’s Nile-Red Sea canals: chronology, location, seasonality and function. In Red Sea IV: Connected Hinterlands (eds Blue, L., Cooper, J., Thomas, R. & Whitewright, J.) 195–210 (Archaeopress, 2009).

Prendergast ME, et al. Reconstructing Asian faunal introductions to eastern Africa from multi-proxy biomolecular and archaeological datasets. PLoS ONE. 2017;12:e0182565. doi: 10.1371/journal.pone.0182565. PubMed DOI PMC

Tollenaere C, et al. Phylogeography of the introduced species Rattus rattus in the western Indian Ocean, with special emphasis on the colonization history of Madagascar. J. Biogeogr. 2010;37:398–410. doi: 10.1111/j.1365-2699.2009.02228.x. DOI

Cobb M. The chronology of Roman Trade in the Indian Ocean from Augustus to early third century ce. J. Econ. Soc. Hist. Orient. 2015;58:362–418. doi: 10.1163/15685209-12341378. DOI

Ewer RF. The biology and behaviour of a free-living population of black rats (Rattus rattus) Anim. Behav. Monogr. 1971;4:127–174. doi: 10.1016/S0066-1856(71)80002-X. DOI

Pocock MJO, Hauffe HC, Searle JB. Dispersal in house mice. Biol. J. Linn. Soc. Lond. 2005;84:565–583. doi: 10.1111/j.1095-8312.2005.00455.x. DOI

Büntgen U, et al. Cooling and societal change during the Late Antique Little Ice Age from 536 to around 660 AD. Nat. Geosci. 2016;9:231–236. doi: 10.1038/ngeo2652. DOI

Perry RD, Fetherston JD. Yersinia pestis-etiologic agent of plague. Clin. Microbiol. Rev. 1997;10:35–66. doi: 10.1128/CMR.10.1.35. PubMed DOI PMC

Spyrou MA, Bos KI, Herbig A, Krause J. Ancient pathogen genomics as an emerging tool for infectious disease research. Nat. Rev. Genet. 2019;20:323–340. doi: 10.1038/s41576-019-0119-1. PubMed DOI PMC

Fenwick C. From Africa to Ifrīqiya: settlement and society in early Medieval North Africa (650–800) Al-Masāq. 2013;25:9–33. doi: 10.1080/09503110.2013.767008. DOI

Pickrell JK, Pritchard JK. Inference of population splits and mixtures from genome-wide allele frequency data. PLoS Genet. 2012;8:e1002967. doi: 10.1371/journal.pgen.1002967. PubMed DOI PMC

McCormick M. Where do trading towns come from? Early medieval Venice and the northern emporia. Post-Rom. towns, trade Settl. Eur. Byzantium. 2007;1:41–68.

Smith D, Kenward H. Roman grain pests in Britain: implications for grain supply and agricultural production. Britannia. 2011;42:243–262. doi: 10.1017/S0068113X11000031. DOI

Buffon, G.-L. L. C. de. Histoire Naturelle, Générale et Particuliére, avec la Description du Cabinet du Roi, Vol. 8 (L’Imprimerie Royale, 1760).

Smith, R. The Universal Directory for Taking Alive and Destroying Rats, and All Other Kinds of Four-footed and Winged Vermin, In a Method Hitherto Unattempted: Calculated for the Use of the Gentleman, the Farmer, and the Warrener (J. Walker, 1768).

Pennant, T. British Zoology (William Eyres, 1776).

Rutty, J. An Essay Towards a Natural History of the County of Dublin, Vol. 1 (W. Sleater, 1772).

O’Connor, T. Commensal species. In The Oxford Handbook of Animal Studies (ed. Kalof, L.) (Oxford University Press, 2017).

Walker T, Sharpe JR, Williams H. Barn owls and black rats from a rural Roman Villa at Gatehampton, South Oxfordshire. Environ. Archaeol. 2021;26:487–496. doi: 10.1080/14614103.2019.1689805. DOI

Ramsey CB. Bayesian analysis of radiocarbon dates. Radiocarbon. 2011;51:337–360. doi: 10.1017/S0033822200033865. DOI

Reimer PJ, Austin WEN, Bard E, Bayliss A. The IntCal20 northern hemisphere radiocarbon age calibration curve (0–55 cal kBP) Radiocarbon. 2020;62:725–757. doi: 10.1017/RDC.2020.41. DOI

Guiry E, Buckley M. Urban rats have less variable, higher protein diets. Proc. R. Soc. B. 2018;285:20181441. doi: 10.1098/rspb.2018.1441. PubMed DOI PMC

Dewar G, Pfeiffer S. Approaches to estimating marine protein in human collagen for radiocarbon date calibration. Radiocarbon. 2010;52:1611–1625. doi: 10.1017/S0033822200056344. DOI

Heaton TJ, et al. Marine20—the marine Radiocarbon Age calibration curve (0–55,000 cal BP) Radiocarbon. 2020;62:779–820. doi: 10.1017/RDC.2020.68. DOI

Chapman JA, et al. Meraculous: de novo genome assembly with short paired-end reads. PLoS ONE. 2011;6:e23501. doi: 10.1371/journal.pone.0023501. PubMed DOI PMC

Smit, AFA, Hubley, R & Green, P. RepeatMasker Open-4.0. http://www.repeatmasker.org (2013–2015).

Benson G. Tandem repeats finder: a program to analyze DNA sequences. Nucleic Acids Res. 1999;27:573–580. doi: 10.1093/nar/27.2.573. PubMed DOI PMC

Kurtz S, et al. Versatile and open software for comparing large genomes. Genome Biol. 2004;5:R12. doi: 10.1186/gb-2004-5-2-r12. PubMed DOI PMC

Dabney J, et al. Complete mitochondrial genome sequence of a Middle Pleistocene cave bear reconstructed from ultrashort DNA fragments. Proc. Natl Acad. Sci. USA. 2013;110:15758–15763. doi: 10.1073/pnas.1314445110. PubMed DOI PMC

Damgaard PB, et al. Improving access to endogenous DNA in ancient bones and teeth. Sci. Rep. 2015;5:11184. doi: 10.1038/srep11184. PubMed DOI PMC

Yang DY, Eng B, Waye JS, Dudar JC, Saunders SR. Technical note: improved DNA extraction from ancient bones using silica-based spin columns. Am. J. Phys. Anthropol. 1998;105:539–543. doi: 10.1002/(SICI)1096-8644(199804)105:4<539::AID-AJPA10>3.0.CO;2-1. PubMed DOI

Speller CF, et al. Ancient mitochondrial DNA analysis reveals complexity of indigenous North American Turkey domestication. Proc. Natl Acad. Sci. USA. 2010;107:2807–2812. doi: 10.1073/pnas.0909724107. PubMed DOI PMC

Rohland N, Harney E, Mallick S, Nordenfelt S, Reich D. Partial uracil–DNA–glycosylase treatment for screening of ancient DNA. Philos. Trans. R. Soc. Lond. B Biol. Sci. 2015;370:20130624. doi: 10.1098/rstb.2013.0624. PubMed DOI PMC

Gansauge, M.-T., Aximu-Petri, A., Nagel, S. & Meyer, M. Manual and automated preparation of single-stranded DNA libraries for the sequencing of DNA from ancient biological remains and other sources of highly degraded DNA. Nat. Protoc. 10.1038/s41596-020-0338-0 (2020). PubMed

Kircher M, Sawyer S, Meyer M. Double indexing overcomes inaccuracies in multiplex sequencing on the Illumina platform. Nucleic Acids Res. 2012;40:e3. doi: 10.1093/nar/gkr771. PubMed DOI PMC

Carøe C, et al. Single‐tube library preparation for degraded DNA. Methods Ecol. Evol. 2018;9:410–419. doi: 10.1111/2041-210X.12871. DOI

Peltzer A, et al. EAGER: efficient ancient genome reconstruction. Genome Biol. 2016;17:60. doi: 10.1186/s13059-016-0918-z. PubMed DOI PMC

Schubert M, Lindgreen S, Orlando L. AdapterRemoval v2: rapid adapter trimming, identification, and read merging. BMC Res. Notes. 2016;9:88. doi: 10.1186/s13104-016-1900-2. PubMed DOI PMC

Li H, Durbin R. Fast and accurate short read alignment with Burrows–Wheeler transform. Bioinformatics. 2009;25:1754–1760. doi: 10.1093/bioinformatics/btp324. PubMed DOI PMC

Jónsson H, Ginolhac A, Schubert M, Johnson PLF, Orlando L. mapDamage2.0: fast approximate Bayesian estimates of ancient DNA damage parameters. Bioinformatics. 2013;29:1682–1684. doi: 10.1093/bioinformatics/btt193. PubMed DOI PMC

Jun G, Wing MK, Abecasis GR, Kang HM. An efficient and scalable analysis framework for variant extraction and refinement from population-scale DNA sequence data. Genome Res. 2015;25:918–925. doi: 10.1101/gr.176552.114. PubMed DOI PMC

Teng H, et al. Population genomics reveals speciation and introgression between Brown Norway rats and their sibling species. Mol. Biol. Evol. 2017;34:2214–2228. doi: 10.1093/molbev/msx157. PubMed DOI PMC

McKenna A, et al. The Genome Analysis Toolkit: a MapReduce framework for analyzing next-generation DNA sequencing data. Genome Res. 2010;20:1297–1303. doi: 10.1101/gr.107524.110. PubMed DOI PMC

Korneliussen TS, Albrechtsen A, Nielsen R. ANGSD: analysis of next generation sequencing data. BMC Bioinforma. 2014;15:356. doi: 10.1186/s12859-014-0356-4. PubMed DOI PMC

Li H. Improving SNP discovery by base alignment quality. Bioinformatics. 2011;27:1157–1158. doi: 10.1093/bioinformatics/btr076. PubMed DOI PMC

Li H, et al. The Sequence Alignment/Map format and SAMtools. Bioinformatics. 2009;25:2078–2079. doi: 10.1093/bioinformatics/btp352. PubMed DOI PMC

Renaud G, Slon V, Duggan AT, Kelso J. Schmutzi: estimation of contamination and endogenous mitochondrial consensus calling for ancient DNA. Genome Biol. 2015;16:224. doi: 10.1186/s13059-015-0776-0. PubMed DOI PMC

Edgar RC. MUSCLE: multiple sequence alignment with high accuracy and high throughput. Nucleic Acids Res. 2004;32:1792–1797. doi: 10.1093/nar/gkh340. PubMed DOI PMC

Darriba D, Taboada GL, Doallo R, Posada D. jModelTest 2: more models, new heuristics and parallel computing. Nat. Methods. 2012;9:772. doi: 10.1038/nmeth.2109. PubMed DOI PMC

Stamatakis A. RAxML version 8: a tool for phylogenetic analysis and post-analysis of large phylogenies. Bioinformatics. 2014;30:1312–1313. doi: 10.1093/bioinformatics/btu033. PubMed DOI PMC

Katoh K, Standley DM. MAFFT multiple sequence alignment software version 7: improvements in performance and usability. Mol. Biol. Evol. 2013;30:772–780. doi: 10.1093/molbev/mst010. PubMed DOI PMC

Purcell S, et al. PLINK: a tool set for whole-genome association and population-based linkage analyses. Am. J. Hum. Genet. 2007;81:559–575. doi: 10.1086/519795. PubMed DOI PMC

Patterson N, et al. Ancient admixture in human history. Genetics. 2012;192:1065–1093. doi: 10.1534/genetics.112.145037. PubMed DOI PMC

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