Sanne Boessenkool
American Museum of Natural History
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Featured researches published by Sanne Boessenkool.
Science | 2012
Laura Parducci; Tina Jørgensen; Mari Mette Tollefsrud; Ellen Elverland; Torbjørn Alm; Sonia L. Fontana; Keith Bennett; James Haile; Irina Matetovici; Yoshihisa Suyama; Mary E. Edwards; Kenneth Geving Andersen; Morten Rasmussen; Sanne Boessenkool; Eric Coissac; Christian Brochmann; Pierre Taberlet; Michael Houmark-Nielsen; Nicolaj K. Larsen; Ludovic Orlando; M. Thomas P. Gilbert; Kurt H. Kjær; Inger Greve Alsos
Tree Refugia Ideas of how and when boreal plants spread to the formerly glaciated parts of the world following the retreat of the glaciers 9000 years ago are long debated. Models of the postglacial spread of boreal plants argue for dispersal from southern refugia; however, Parducci et al. (p. 1083) have shown that both spruce and pine were present in small ice-free regions of Scandinavia much earlier than thought. DNA haplotyping confirmed that a remnant mitochondrial type of spruce, once unique to Scandinavia, now lives alongside the more common spruce originating from Eastern Europe. Evidence from lake cores collected from central and northern Norway indicated the survival of conifers as early as 22,000 years before the present, when apart from ice-free pockets, most of Scandinavia was covered by ice. DNA from modern and ancient spruce and pine indicate that both survived in ice-free areas during the last glaciations. It is commonly believed that trees were absent in Scandinavia during the last glaciation and first recolonized the Scandinavian Peninsula with the retreat of its ice sheet some 9000 years ago. Here, we show the presence of a rare mitochondrial DNA haplotype of spruce that appears unique to Scandinavia and with its highest frequency to the west—an area believed to sustain ice-free refugia during most of the last ice age. We further show the survival of DNA from this haplotype in lake sediments and pollen of Trøndelag in central Norway dating back ~10,300 years and chloroplast DNA of pine and spruce in lake sediments adjacent to the ice-free Andøya refugium in northwestern Norway as early as ~22,000 and 17,700 years ago, respectively. Our findings imply that conifer trees survived in ice-free refugia of Scandinavia during the last glaciation, challenging current views on survival and spread of trees as a response to climate changes.
Nature | 2014
John Davison; Mari Moora; Martin Zobel; Eric Coissac; Mary E. Edwards; Eline D. Lorenzen; Mette Vestergård; Galina Gussarova; James Haile; Joseph M. Craine; Ludovic Gielly; Sanne Boessenkool; Laura Saskia Epp; Rachid Cheddadi; David W. Murray; Kari Anne Bråthen; Nigel G. Yoccoz; Heather Binney; Corinne Cruaud; Patrick Wincker; Tomasz Goslar; Inger Greve Alsos; Eva Bellemain; Anne K. Brysting; Reidar Elven; J. H. Sønstebø; Julian B. Murton; Andrei Sher; Morten Rasmussen; Regin Rønn
Although it is generally agreed that the Arctic flora is among the youngest and least diverse on Earth, the processes that shaped it are poorly understood. Here we present 50 thousand years (kyr) of Arctic vegetation history, derived from the first large-scale ancient DNA metabarcoding study of circumpolar plant diversity. For this interval we also explore nematode diversity as a proxy for modelling vegetation cover and soil quality, and diets of herbivorous megafaunal mammals, many of which became extinct around 10 kyr bp (before present). For much of the period investigated, Arctic vegetation consisted of dry steppe-tundra dominated by forbs (non-graminoid herbaceous vascular plants). During the Last Glacial Maximum (25–15 kyr bp), diversity declined markedly, although forbs remained dominant. Much changed after 10 kyr bp, with the appearance of moist tundra dominated by woody plants and graminoids. Our analyses indicate that both graminoids and forbs would have featured in megafaunal diets. As such, our findings question the predominance of a Late Quaternary graminoid-dominated Arctic mammoth steppe.
Molecular Ecology | 2012
Laura Saskia Epp; Sanne Boessenkool; Eva Bellemain; James Haile; Alfonso Esposito; Tiayyba Riaz; Christer Erséus; Vladimir I. Gusarov; Mary E. Edwards; Arild Johnsen; Hans K. Stenøien; Kristian Hassel; Håvard Kauserud; Nigel G. Yoccoz; Kari Anne Bråthen; Pierre Taberlet; Eric Coissac; Christian Brochmann
Metabarcoding approaches use total and typically degraded DNA from environmental samples to analyse biotic assemblages and can potentially be carried out for any kinds of organisms in an ecosystem. These analyses rely on specific markers, here called metabarcodes, which should be optimized for taxonomic resolution, minimal bias in amplification of the target organism group and short sequence length. Using bioinformatic tools, we developed metabarcodes for several groups of organisms: fungi, bryophytes, enchytraeids, beetles and birds. The ability of these metabarcodes to amplify the target groups was systematically evaluated by (i) in silico PCRs using all standard sequences in the EMBL public database as templates, (ii) in vitro PCRs of DNA extracts from surface soil samples from a site in Varanger, northern Norway and (iii) in vitro PCRs of DNA extracts from permanently frozen sediment samples of late‐Pleistocene age (∼16 000–50 000 years bp) from two Siberian sites, Duvanny Yar and Main River. Comparison of the results from the in silico PCR with those obtained in vitro showed that the in silico approach offered a reliable estimate of the suitability of a marker. All target groups were detected in the environmental DNA, but we found large variation in the level of detection among the groups and between modern and ancient samples. Success rates for the Pleistocene samples were highest for fungal DNA, whereas bryophyte, beetle and bird sequences could also be retrieved, but to a much lesser degree. The metabarcoding approach has considerable potential for biodiversity screening of modern samples and also as a palaeoecological tool.
Molecular Ecology | 2012
Tine Jørgensen; James Haile; Per Möller; Andrei Andreev; Sanne Boessenkool; Morten Rasmussen; Frank Kienast; Eric Coissac; Pierre Taberlet; Christian Brochmann; Nancy H. Bigelow; Khenrik Sune Andersen; Ludovic Orlando; Mpt Gilbert
Although ancient DNA from sediments (sedaDNA) has been used to investigate past ecosystems, the approach has never been directly compared with the traditional methods of pollen and macrofossil analysis. We conducted a comparative survey of 18 ancient permafrost samples spanning the Late Pleistocene (46–12.5 thousand years ago), from the Taymyr Peninsula in northern Siberia. The results show that pollen, macrofossils and sedaDNA are complementary rather than overlapping and, in combination, reveal more detailed information on plant palaeocommunities than can be achieved by each individual approach. SedaDNA and macrofossils share greater overlap in plant identifications than with pollen, suggesting that sedaDNA is local in origin. These two proxies also permit identification to lower taxonomic levels than pollen, enabling investigation into temporal changes in species composition and the determination of indicator species to describe environmental changes. Combining data from all three proxies reveals an area continually dominated by a mosaic vegetation of tundra‐steppe, pioneer and wet‐indicator plants. Such vegetational stability is unexpected, given the severe climate changes taking place in the Northern Hemisphere during this time, with changes in average annual temperatures of >22 °C. This may explain the abundance of ice‐age mammals such as horse and bison in Taymyr Peninsula during the Pleistocene and why it acted as a refugium for the last mainland woolly mammoth. Our finding reveals the benefits of combining sedaDNA, pollen and macrofossil for palaeovegetational reconstruction and adds to the increasing evidence suggesting large areas of the Northern Hemisphere remained ecologically stable during the Late Pleistocene.
Conservation Genetics | 2007
Sanne Boessenkool; Sabrina S. Taylor; Carolyn K. Tepolt; Jan Komdeur; Ian G. Jamieson
For conservation purposes islands are considered safe refuges for many species, particularly in regions where introduced predators form a major threat to the native fauna, but island populations are also known to possess low levels of genetic diversity. The New Zealand archipelago provides an ideal system to compare genetic diversity of large mainland populations where introduced predators are common, to that of smaller offshore islands, which serve as predator-free refuges. We assessed microsatellite variation in South Island robins (Petroica australis australis), and compared large mainland, small mainland, natural island and translocated island populations. Large mainland populations exhibited more polymorphic loci and higher number of alleles than small mainland and natural island populations. Genetic variation did not differ between natural and translocated island populations, even though one of the translocated populations was established with five individuals. Hatching failure was recorded in a subset of the populations and found to be significantly higher in translocated populations than in a large mainland population. Significant population differentiation was largely based on heterogeneity in allele frequencies (including fixation of alleles), as few unique alleles were observed. This study shows that large mainland populations retain higher levels of genetic diversity than natural and translocated island populations. It highlights the importance of protecting these mainland populations and using them as a source for new translocations. In the future, these populations may become extremely valuable for species conservation if existing island populations become adversely affected by low levels of genetic variation and do not persist.
Molecular Ecology | 2012
Sanne Boessenkool; Laura Saskia Epp; James Haile; Eva Bellemain; Mary E. Edwards; Eric Coissac; Christian Brochmann
Analyses of degraded DNA are typically hampered by contamination, especially when employing universal primers such as commonly used in environmental DNA studies. In addition to false‐positive results, the amplification of contaminant DNA may cause false‐negative results because of competition, or bias, during the PCR. In this study, we test the utility of human‐specific blocking primers in mammal diversity analyses of ancient permafrost samples from Siberia. Using quantitative PCR (qPCR) on human and mammoth DNA, we first optimized the design and concentration of blocking primer in the PCR. Subsequently, 454 pyrosequencing of ancient permafrost samples amplified with and without the addition of blocking primer revealed that DNA sequences from a diversity of mammalian representatives of the Beringian megafauna were retrieved only when the blocking primer was added to the PCR. Notably, we observe the first retrieval of woolly rhinoceros (Coelodonta antiquitatis) DNA from ancient permafrost cores. In contrast, reactions without blocking primer resulted in complete dominance by human DNA sequences. These results demonstrate that in ancient environmental analyses, the PCR can be biased towards the amplification of contaminant sequences to such an extent that retrieval of the endogenous DNA is severely restricted. The application of blocking primers is a promising tool to avoid this bias and can greatly enhance the quantity and the diversity of the endogenous DNA sequences that are amplified.
Environmental Microbiology | 2013
Eva Bellemain; Marie L. Davey; Håvard Kauserud; Laura Saskia Epp; Sanne Boessenkool; Eric Coissac; József Geml; Mary E. Edwards; Galina Gussarova; Pierre Taberlet; Christian Brochmann
The taxonomic and ecological diversity of ancient fungal communities was assessed by combining next generation sequencing and metabarcoding of DNA preserved in permafrost. Twenty-six sediment samples dated 16 000-32 000 radiocarbon years old from two localities in Siberia were analysed for fungal ITS. We detected 75 fungal OTUs from 21 orders representing three phyla, although rarefaction analyses suggested that the full diversity was not recovered despite generating an average of 6677 ± 3811 (mean ± SD) sequences per sample and that preservation bias likely has considerable effect on the recovered DNA. Most OTUs (75.4%) represented ascomycetes. Due to insufficient sequencing depth, DNA degradation and putative preservation biases in our samples, the recovered taxa probably do not represent the complete historic fungal community, and it is difficult to determine whether the fungal communities varied geographically or experienced a composition shift within the period of 16 000-32 000 bp. However, annotation of OTUs to functional ecological groups provided a wealth of information on the historic communities. About one-third of the OTUs are presumed plant-associates (pathogens, saprotrophs and endophytes) typical of graminoid- and forb-rich habitats. We also detected putative insect pathogens, coprophiles and keratinophiles likely associated with ancient insect and herbivore faunas. The detection of putative insect pathogens, mycoparasites, aquatic fungi and endophytes broadens our previous knowledge of the diversity of fungi present in Beringian palaeoecosystems. A large group of putatively psychrophilic/psychrotolerant fungi was also detected, most likely representing a modern, metabolically active fungal community.
Molecular Ecology | 2012
Tina Jørgensen; Kurt H. Kjær; James Haile; Morten Rasmussen; Sanne Boessenkool; Kenneth Geving Andersen; Eric Coissac; Pierre Taberlet; Christian Brochmann; Ludovic Orlando; M. Thomas P. Gilbert
Nunataks are isolated bedrocks protruding through ice sheets. They vary in age, but represent island environments in ‘oceans’ of ice through which organism dispersals and replacements can be studied over time. The J.A.D. Jensen’s Nunataks at the southern Greenland ice sheet are the most isolated nunataks on the northern hemisphere – some 30 km from the nearest biological source. They constitute around 2 km2 of ice‐free land that was established in the early Holocene. We have investigated the changes in plant composition at these nunataks using both the results of surveys of the flora over the last 130 years and through reconstruction of the vegetation from the end of the Holocene Thermal Maximum (5528 ± 75 cal year BP) using meta‐barcoding of plant DNA recovered from the nunatak sediments (sedaDNA). Our results show that several of the plant species detected with sedaDNA are described from earlier vegetation surveys on the nunataks (in 1878, 1967 and 2009). In 1967, a much higher biodiversity was detected than from any other of the studied periods. While this may be related to differences in sampling efforts for the oldest period, it is not the case when comparing the 1967 and 2009 levels where the botanical survey was exhaustive. As no animals and humans are found on the nunataks, this change in diversity over a period of just 42 years must relate to environmental changes probably being climate‐driven. This suggests that even the flora of fairly small and isolated ice‐free areas reacts quickly to a changing climate.
Conservation Biology | 2014
Sanne Boessenkool; Gayle Mcglynn; Laura Saskia Epp; David Taylor; Manuel Pimentel; Abel Gizaw; Sileshi Nemomissa; Christian Brochmann; Magnus Popp
Conservation of biodiversity may in the future increasingly depend upon the availability of scientific information to set suitable restoration targets. In traditional paleoecology, sediment-based pollen provides a means to define preanthropogenic impact conditions, but problems in establishing the exact provenance and ecologically meaningful levels of taxonomic resolution of the evidence are limiting. We explored the extent to which the use of sedimentary ancient DNA (sedaDNA) may complement pollen data in reconstructing past alpine environments in the tropics. We constructed a record of afro-alpine plants retrieved from DNA preserved in sediment cores from 2 volcanic crater sites in the Albertine Rift, eastern Africa. The record extended well beyond the onset of substantial anthropogenic effects on tropical mountains. To ensure high-quality taxonomic inference from the sedaDNA sequences, we built an extensive DNA reference library covering the majority of the afro-alpine flora, by sequencing DNA from taxonomically verified specimens. Comparisons with pollen records from the same sediment cores showed that plant diversity recovered with sedaDNA improved vegetation reconstructions based on pollen records by revealing both additional taxa and providing increased taxonomic resolution. Furthermore, combining the 2 measures assisted in distinguishing vegetation change at different geographic scales; sedaDNA almost exclusively reflects local vegetation, whereas pollen can potentially originate from a wide area that in highlands in particular can span several ecozones. Our results suggest that sedaDNA may provide information on restoration targets and the nature and magnitude of human-induced environmental changes, including in high conservation priority, biodiversity hotspots, where understanding of preanthropogenic impact (or reference) conditions is highly limited.
Molecular Ecology | 2009
Sanne Boessenkool; Bastiaan Star; Jonathan M. Waters; Philip J. Seddon
The identification of demographically independent populations and the recognition of management units have been greatly facilitated by the continuing advances in genetic tools. Managements units now play a key role in short‐term conservation management programmes of declining species, but their importance in expanding populations receives comparatively little attention. The endangered yellow‐eyed penguin (Megadyptes antipodes) expanded its range from the subantarctic to New Zealands South Island a few hundred years ago and this new population now represents almost half of the species’ total census size. This dramatic expansion attests to M. antipodes’ high dispersal abilities and suggests the species is likely to constitute a single demographic population. Here we test this hypothesis of panmixia by investigating genetic differentiation and levels of gene flow among penguin breeding areas using 12 autosomal microsatellite loci along with mitochondrial control region sequence analyses for 350 individuals. Contrary to our hypothesis, however, the analyses reveal two genetically and geographically distinct assemblages: South Island vs. subantarctic populations. Using assignment tests, we recognize just two first‐generation migrants between these populations (corresponding to a migration rate of < 2%), indicating that ongoing levels of long‐distance migration are low. Furthermore, the South Island population has low genetic variability compared to the subantarctic population. These results suggest that the South Island population was founded by only a small number of individuals, and that subsequent levels of gene flow have remained low. The demographic independence of the two populations warrants their designation as distinct management units and conservation efforts should be adjusted accordingly to protect both populations.