Search

It is increasingly common for apex predators to face a multitude of complex conservation issues. In Australia, dingoes are the mainland apex predator and play an important role in ecological functioning. Currently, however, they are threatened by hybridization with modern domestic dogs in the wild. As a consequence, we explore how increasing our understanding of the evolutionary history of dingoes can inform management and conservation decisions. Previous research on whole mitochondrial genome and nuclear data from five geographical populations showed evidence of two distinct lineages of dingo. Here, we present data from a broader survey of dingoes around Australia using both mitochondrial and Y chromosome markers and investigate the timing of demographic expansions. Biogeographic data corroborate the presence of at least two geographically subdivided genetic populations, southeastern and northwestern. Demographic modeling suggests that dingoes have undergone population expansion in the last 5,000 years. It is not clear whether this stems from expansion into vacant niches after the extinction of thylacines on the mainland or indicates the arrival date of dingoes. Male dispersal is much more common than female, evidenced by more diffuse Y haplogroup distributions. There is also evidence of likely historical male biased introgression from domestic dogs into dingoes, predominately within southeastern Australia. These findings have critical practical implications for the management and conservation of dingoes in Australia; particularly a focus must be placed upon the threatened southeastern dingo population.

Domestic dogs have been central to life in the North American Arctic for millennia. The ancestors of the Inuit were the first to introduce the widespread usage of dog sledge transportation technology to the Americas, but whether the Inuit adopted local Palaeo-Inuit dogs or introduced a new dog population to the region remains unknown. To test these hypotheses, we generated mitochondrial DNA and geometric morphometric data of skull and dental elements from a total of 922 North American Arctic dogs and wolves spanning over 4500 years. Our analyses revealed that dogs from Inuit sites dating from 2000 BP possess morphological and genetic signatures that distinguish them from earlier Palaeo-Inuit dogs, and identified a novel mitochondrial clade in eastern Siberia and Alaska. The genetic legacy of these Inuit dogs survives today in modern Arctic sledge dogs despite phenotypic differences between archaeological and modern Arctic dogs. Together, our data reveal that Inuit dogs derive from a secondary pre-contact migration of dogs distinct from Palaeo-Inuit dogs, and probably aided the Inuit expansion across the North American Arctic beginning around 1000 BP. Domestic dogs have been central to life in the North American Arctic for millennia. The ancestors of the Inuit were the first to introduce the widespread usage of dog sledge transportation technology to the Americas, but whether the Inuit adopted local Palaeo-Inuit dogs or introduced a new dog population to the region remains unknown. To test these hypotheses, we generated mitochondrial DNA and geometric morphometric data of skull and dental elements from a total of 922 North American Arctic dogs and wolves spanning over 4500 years. Our analyses revealed that dogs from Inuit sites dating from 2000 BP possess morphological and genetic signatures that distinguish them from earlier Palaeo-Inuit dogs, and identified a novel mitochondrial clade in eastern Siberia and Alaska. The genetic legacy of these Inuit dogs survives today in modern Arctic sledge dogs despite phenotypic differences between archaeological and modern Arctic dogs. Together, our data reveal that Inuit dogs derive from a secondary pre-contact migration of dogs distinct from Palaeo-Inuit dogs, and probably aided the Inuit expansion across the North American Arctic beginning around 1000 BP.

Species have been shaped by past environmental conditions. Ancient remnants of species (bones, teeth, coprolites, pollen, shed cells, etc.) with preserved DNA (deoxyribonucleic acid) can reveal responses to past environmental changes through genetic information in the form of ancient DNA. Here we review the uses of ancient DNA to gain insights into ecological and evolutionary processes by investigating: (1) how climate has affected population dynamics through time, (2) how species react differently to climate change, (3) what triggers extinction for some species, (4) the detection of genomic adaptation to the environment and (5) how ancient DNA can be used to reconstruct past environmental conditions/habitats. The details that we can glean from past responses to climate change will provide information on how we can expect species to respond to future climate change. Key Concepts Ancient DNA (aDNA) can be utilised to infer how species reacted to past ecological changes. Populations are dynamic and respond to past climate change in many ways; through population size change, altered distributions and migrations. In combination with environmental data, ancient DNA is helping to elucidate what drove some species to extinction. Species have adapted to past climates. Ancient DNA, primarily through candidate gene searches, has revealed the genes behind these adaptations. Indirect methods of sampling soil for ancient DNA has aided in reconstructing past habitats. Ancient DNA can decipher how species responded to past natural climate change. This information can be used to aid in conservation. Keywords: ancient DNA; demography; adaptation; climate change; extinction

Volcanoes can produce far-reaching hazards that extend distances of tens or hundreds of kilometres in large eruptions, or in certain conditions for smaller eruptions. About a tenth of the world’s population lives within the potential footprint of volcanic hazards and lives are regularly lost through volcanic activity: volcanic fatalities were recorded in 18 of the last 20 years. This paper identifies the distance and distribution of fatalities around volcanoes and the activities of the victims at the time of impact, sourced from an extensive search of academic and grey literature, including media and official reports. We update and expand a volcano fatality database to include all data from 1500 AD to 2017. This database contains 635 records of 278,368 fatalities. Each record contains information on the number of fatalities, fatal cause, incident date and the fatality location in terms of distance from the volcano. Distance data were previously available in just 5% of fatal incidents: these data have been significantly increased to 72% (456/635) of fatal incidents, with fatalities recorded from inside the crater to more than 100 km from the summit. Local residents are the most frequently killed, but tourists, volcanologists and members of the media are also identified as common victims. These latter groups and residents of small islands dominate the proximal fatality record up to 5 km from the volcano. Though normally accounting for small numbers of fatalities, ballistics are the most common cause of fatal incidents at this distance. Pyroclastic density currents are the dominant fatal cause at 5 to 15 km. Lahars, tsunami and tephra dominate the record after about 15 km. The new location data are used to characterise volcanic threat with distance, as a function of eruption size and hazard type, and to understand how certain activities increase exposure and the likelihood of death. These findings support assessment of volcanic threat, population exposure and vulnerabilities related to occupation or activity. Published version

Domesticated animals that revert to a wild state can become invasive and significantly impact native biodiversity. Although dogs can be problematic locally, only the Australasian dingo is known to occur in isolation from humans. Western dogs have experienced more intense artificial selection, which potentially limits their invasiveness. However, feral dogs eradicated from Isabela Island, Galápagos in the 1980s could be the first-known exception. We used DNA and morphometric data from 92 of these dogs to test the hypotheses that (i) these dogs persisted independently of humans for up to a century and a half since descending from a handful of dogs introduced in the early 1800s, vs. (ii) similarly to other western feral dog populations, they reflected continuous recruitment of strays from human settlements on a portion of the Island. We detected one dominant maternal lineage and one dominant paternal lineage shared by the three subpopulations, along with low autosomal genetic diversity, consistent with the hypothesized common origins from a small founder population. Genetic diversity patterns among the three island subpopulations were consistent with stepping-stone founder effects, while morphometric differentiation suggested rapid phenotypic divergence, possibly due to drift and reinforced by selection corresponding to distinct microclimates and habitats on Isabela. Despite the continued presence of free-ranging dogs in the vicinity of settlements on Isabela and other Galápagos Islands, feral populations have not reestablished in remote areas since the 1980s, emphasizing the rarity of conditions necessary for feralization of modern western dogs.

Throughout most of the Americas, post-colonial dogs largely erased the genetic signatures of pre-historical dogs. However, the North American Arctic harbors dogs that are potentially descended from pre-historical ancestors, as well as those affected by post-colonial translocations and admixtures. In particular, Inuit dogs from Canada and Greenland are thought to descend from dogs associated with Thule peoples, who relied on them for transportation ca. 1000 years ago. Whether Thule dogs reflected an earlier colonization by Paleoeskimo dogs ca. 4500 years ago is unknown. During the Alaskan Gold Rush, additional sled dogs, possibly of post-colonial derivation, the Alaskan Husky, Malamute and Siberian Husky, were used in the Arctic. The genealogical relationships among and origins of these breeds are unknown. Here we use autosomal, paternal and maternal DNA markers to (1) test the hypothesis that Inuit dogs have retained their indigenous ancestry, (2) characterize their relationship to one another and to other Arctic breeds, and (3) estimate the age of North American indigenous matrilines and patrilines. On the basis of the agreement of all three markers we determined that Inuit dogs have maintained their indigenous nature, and that they likely derive from Thule dogs. In addition, we provide support for previous research that the Inuit dogs from Canada and Greenland dog should not be distinguished as two breeds. The Alaskan Husky displayed evidence of European introgression, in contrast to the Malamute and Siberian Husky, which appear to have maintained most of their ancient Siberian ancestry.

The dusky-footed woodrat (Neotoma fuscipes) is an endemic North American rodent belonging to the family Cricetidae. We present here the first complete mitogenome within the Neotoma genus. The mitogenome is 16,199 bp in length, and has a structure and gene organization similar to other rodent species (e.g. Mus musculus, Peromyscus maniculatus and Microtus fortis calamorum). The overall base composition is A (35.2%), C (25.5%), G (12.3%), T (27.0%), with a GC content of 37.8%, similar to other rodents. This mitogenome serves as a foundation for future phylogenetic, phylogeographic and population genetic studies.

Dogs originated more than 14,000 BP, but the location(s) where they first arose is uncertain. The earliest archeological evidence of ancient dogs was discovered in Europe and the Middle East, some 5-7 millennia before that from Southeast Asia. However, mitochondrial DNA analyses suggest that most modern dogs derive from Southeast Asia, which has fueled the controversial hypothesis that dog domestication originated in this region despite the lack of supporting archeological evidence. We propose and investigate with Y chromosomes an alternative hypothesis for the proximate origins of dogs from Southeast Asia--a massive Neolithic expansion of dogs from this region that largely replaced more primitive dogs to the west and north. Previous attempts to test matrilineal findings with independent patrilineal markers have lacked the necessary genealogical resolution and mutation rate estimates. Here, we used Y chromosome genotypes, composed of 29 single-nucleotide polymorphism (SNPs) and 5 single tandem repeats (STRs), from 338 Australian dingoes, New Guinea singing dogs, and village dogs from Island Southeast Asia, along with modern European breed dogs, to estimate the evolutionary mutation rates of Y chromosome STRs based on calibration to the independently known age of the dingo population. Dingoes exhibited a unique haplogroup characterized by a single distinguishing SNP mutation and 14 STR haplotypes. The age of the European haplogroup was estimated to be only 1.7 times older than that of the dingo population, suggesting an origin during the Neolithic rather than the Paleolithic (as predicted by the Southeast Asian origins hypothesis). We hypothesize that isolation of Neolithic dogs from wolves in Southeast Asia was a key step accelerating their phenotypic transformation, enhancing their value in trade and as cargo, and enabling them to rapidly expand and replace more primitive dogs to the West. Our findings also suggest that dingoes could have arrived in Australia directly from Taiwan, independently of later dispersals of dogs through Thailand to Island Southeast Asia.

To facilitate the assessment of hazards and risk from volcanoes, we have created a comprehensive global database of Quaternary Large Magnitude Explosive Volcanic Eruptions (LaMEVE). This forms part of the larger Volcanic Global Risk Identification and Analysis Project (VOGRIPA), and also forms part of the Global Volcano Model (GVM) initiative (http://www.globalvolcanomodel.org). A flexible search tool allows users to select data on a global, regional or local scale; the selected data can be downloaded into a spreadsheet. The database is publically available online at http://www.bgs.ac.uk/vogripa and currently contains information on nearly 3,000 volcanoes and over 1,800 Quaternary eruption records. Not all volcanoes currently have eruptions associated with them but have been included to allow for easy expansion of the database as more data are found. Data fields include: magnitude, Volcanic Explosivity Index (VEI), deposit volumes, eruption dates, and rock type. The scientific community is invited to contribute new data and also alert the database manager to potentially incorrect data. Whilst the database currently focuses only on large magnitude eruptions, it will be expanded to include data specifically relating to the principal volcanic hazards (e.g. pyroclastic flows, tephra fall, lahars, debris avalanches, ballistics), as well as vulnerability (e.g. population figures, building type) to facilitate risk assessments of future eruptions.