Jeremy Austin

Dr. Jeremy Austin


Research Focus & Metrics

Academic Career Length

33Years (1994-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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5 February 2014 in Nature
Verified
Journal Article
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EWEske Willerslev
Eske Willerslev
JDJohn Davison
John Davison
MMMari Moora
Mari Moora
MZMartin Zobel
Martin Zobel
ÉCÉric Coissac
Éric Coissac
PTPierre Taberlet
Pierre Taberlet

30 May 2014 in Molecular Biology and Evolution
Verified
Journal Article
Open access
PDF file
Kieren J. MitchellKieren J. Mitchell
Kieren J. Mitchell
RPRenae C. Pratt
Renae C. Pratt
LWLaura N. Watson
Laura N. Watson
GGGillian C. Gibb
Gillian C. Gibb
Bastien LlamasBastien Llamas
Bastien Llamas
ACAlan Cooper
Alan Cooper
Marsupials exhibit great diversity in ecology and morphology. However, compared with their sister group, the placental mammals, our understanding of many aspects of marsupial evolution remains limited. We use 101 mitochondrial genomes and data from 26 nuclear loci to reconstruct a dated phylogeny including 97% of extant genera and 58% of modern marsupial species. This tree allows us to analyze the evolution of habitat preference and geographic distributions of marsupial species through time. We found a pattern of mesic-adapted lineages evolving to use more arid and open habitats, which is broadly consistent with regional climate and environmental change. However, contrary to the general trend, several lineages subsequently appear to have reverted from drier to more mesic habitats. Biogeographic reconstructions suggest that current views on the connectivity between Australia and New Guinea/Wallacea during the Miocene and Pliocene need to be revised. The antiquity of several endemic New Guinean clades strongly suggests a substantially older period of connection stretching back to the Middle Miocene and implies that New Guinea was colonized by multiple clades almost immediately after its principal formation.

1 February 2001 in Nature
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Journal Article
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ACAlan Cooper
Alan Cooper
CLCarles Lalueza-Fox
Carles Lalueza-Fox
SASimon Anderson
Simon Anderson
ARAndrew Rambaut
Andrew Rambaut
JAJeremy Austin
Jeremy Austin
RWRyk Ward
Ryk Ward

2 November 2011 in PLOS ONE
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Journal Article
Open access
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KAKen P. Aplin
Ken P. Aplin
HSHitoshi Suzuki
Hitoshi Suzuki
ACAlejandro A. Chinen
Alejandro A. Chinen
RCR. Terry Chesser
R. Terry Chesser
JHJosé Ten Have
José Ten Have
ACAlan Cooper
Alan Cooper
The Black Rat (Rattus rattus) spread out of Asia to become one of the world's worst agricultural and urban pests, and a reservoir or vector of numerous zoonotic diseases, including the devastating plague. Despite the global scale and inestimable cost of their impacts on both human livelihoods and natural ecosystems, little is known of the global genetic diversity of Black Rats, the timing and directions of their historical dispersals, and the risks associated with contemporary movements. We surveyed mitochondrial DNA of Black Rats collected across their global range as a first step towards obtaining an historical genetic perspective on this socioeconomically important group of rodents. We found a strong phylogeographic pattern with well-differentiated lineages of Black Rats native to South Asia, the Himalayan region, southern Indochina, and northern Indochina to East Asia, and a diversification that probably commenced in the early Middle Pleistocene. We also identified two other currently recognised species of Rattus as potential derivatives of a paraphyletic R. rattus. Three of the four phylogenetic lineage units within R. rattus show clear genetic signatures of major population expansion in prehistoric times, and the distribution of particular haplogroups mirrors archaeologically and historically documented patterns of human dispersal and trade. Commensalism clearly arose multiple times in R. rattus and in widely separated geographic regions, and this may account for apparent regionalism in their associated pathogens. Our findings represent an important step towards deeper understanding the complex and influential relationship that has developed between Black Rats and humans, and invite a thorough re-examination of host-pathogen associations among Black Rats.

22 August 2007 in Nucleic Acids Research
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Journal Article
Open access
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PBPaul Brotherton
Paul Brotherton
PEPhillip Endicott
Phillip Endicott
JSJuan J. Sanchez
Juan J. Sanchez
MBMark Beaumont
Mark Beaumont
RBRoss Barnett
Ross Barnett
ACAlan Cooper
Alan Cooper
Ancient DNA (aDNA) research has long depended on the power of PCR to amplify trace amounts of surviving genetic material from preserved specimens. While PCR permits specific loci to be targeted and amplified, in many ways it can be intrinsically unsuited to damaged and degraded aDNA templates. PCR amplification of aDNA can produce highly-skewed distributions with significant contributions from miscoding lesion damage and non-authentic sequence artefacts. As traditional PCR-based approaches have been unable to fully resolve the molecular nature of aDNA damage over many years, we have developed a novel single primer extension (SPEX)-based approach to generate more accurate sequence information. SPEX targets selected template strands at defined loci and can generate a quantifiable redundancy of coverage; providing new insights into the molecular nature of aDNA damage and fragmentation. SPEX sequence data reveals inherent limitations in both traditional and metagenomic PCR-based approaches to aDNA, which can make current damage analyses and correct genotyping of ancient specimens problematic. In contrast to previous aDNA studies, SPEX provides strong quantitative evidence that C > U-type base modifications are the sole cause of authentic endogenous damage-derived miscoding lesions. This new approach could allow ancient specimens to be genotyped with unprecedented accuracy.

29 December 2009 in Proceedings of the National Academy of Sciences
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Journal Article
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JHJames Haile
James Haile
DFDuane G. Froese
Duane G. Froese
RMRoss D. E. MacPhee
Ross D. E. MacPhee
RRRichard G. Roberts
Richard G. Roberts
LALee J. Arnold
Lee J. Arnold
EWEske Willerslev
Eske Willerslev
Causes of late Quaternary extinctions of large mammals (“megafauna”) continue to be debated, especially for continental losses, because spatial and temporal patterns of extinction are poorly known. Accurate latest appearance dates (LADs) for such taxa are critical for interpreting the process of extinction. The extinction of woolly mammoth and horse in northwestern North America is currently placed at 15,000–13,000 calendar years before present (yr BP), based on LADs from dating surveys of macrofossils (bones and teeth). Advantages of using macrofossils to estimate when a species became extinct are offset, however, by the improbability of finding and dating the remains of the last-surviving members of populations that were restricted in numbers or confined to refugia. Here we report an alternative approach to detect ‘ghost ranges’ of dwindling populations, based on recovery of ancient DNA from perennially frozen and securely dated sediments ( sed aDNA). In such contexts, sed aDNA can reveal the molecular presence of species that appear absent in the macrofossil record. We show that woolly mammoth and horse persisted in interior Alaska until at least 10,500 yr BP, several thousands of years later than indicated from macrofossil surveys. These results contradict claims that Holocene survival of mammoths in Beringia was restricted to ecologically isolated high-latitude islands. More importantly, our finding that mammoth and horse overlapped with humans for several millennia in the region where people initially entered the Americas challenges theories that megafaunal extinction occurred within centuries of human arrival or were due to an extraterrestrial impact in the late Pleistocene.