Edvard Glücksman

Edvard Glücksman

Penryn, Cornwall, United Kingdom (Truro, United Kingdom)

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Edvard Glücksman's Overview


500+ connections

Edvard Glücksman's Experience

Associate Research Fellow, Environment and Sustainability Institute

University of Exeter

April 2014Present (6 months) College of Engineering, Mathematics & Physical Sciences

Postdoctoral researcher

University of Duisburg-Essen

January 2013Present (1 year 9 months) Essen Area, Germany

Emerging Leaders in Environmental and Energy Policy Network (ELEEP)

Atlantic Council of the United States

November 2011Present (2 years 11 months) Europe and North America

Edvard Glücksman's Education

University of Oxford


University of Oxford


McGill University


Edvard Glücksman's Publications

  • Novel Virus Discovery and Genome Reconstruction from Field RNA Samples Reveals Highly Divergent Viruses in Dipteran Hosts

    • PLOS ONE
    • November 18, 2013
    Authors: Betty Chung, David Bass, Gregory Moureau, Shuoya Tang, Erica McAlister, Lorna Culverwell, Edvard Glücksman, Hui Wang, T David K Brown, Ernest A. Gould, Ralph E. Harbach

    We investigated whether small RNA (sRNA) sequenced from field-collected mosquitoes and chironomids (Diptera) can be used as a proxy signature of viral prevalence within a range of species and viral groups, using sRNAs sequenced from wild-caught specimens, to inform total RNA deep sequencing of samples of particular interest. Using this strategy, we sequenced from adult Anopheles maculipennis s.l. mosquitoes the apparently nearly complete genome of one previously undescribed virus related to chronic bee paralysis virus, and, from a pool of Ochlerotatus caspius and Oc. detritus mosquitoes, a nearly complete entomobirnavirus genome. We also reconstructed long sequences (1503-6557 nt) related to at least nine other viruses. Crucially, several of the sequences detected were reconstructed from host organisms highly divergent from those in which related viruses have been previously isolated or discovered. It is clear that viral transmission and maintenance cycles in nature are likely to be significantly more complex and taxonomically diverse than previously expected.

  • Phylogeny and evolution of Planomonadida (Sulcozoa): eight new species and new genera Fabomonas and Nutomonas

    • European Journal of Protistology
    • February 2013
    Authors: Edvard Glücksman, Libby Snell, Thomas Cavalier-Smith

    Planomonads are widespread gliding zooflagellates from marine and freshwater sediments with seven species. We cultured 13 new strains; morphology and 18S and ITS2 rDNA sequences show that 11 represent eight new species described here. The 15 species form four robust clades, corresponding to revised Planomonas and Ancyromonas and new genera Fabomonas (marine) and Nutomonas (freshwater). Fabomonas tropica differs in shape and is genetically very distant from previously known planomonads, yet ultrastructurally similar. Anterior cilium morphology maps simply onto the rDNA tree forming the basis for two revised families: Ancyromonadidae (Ancyromonas, Nutomonas) have a uniformly thin, entirely acronematic anterior cilium; Planomonadidae (Fabomonas, Planomonas micra, and new species Planomonas elongata, bulbosa, and brevis) have a
    more conspicuous emergent basal region of the anterior cilium of normal thickness. ITS2 secondary structure is clade-specific, differing most sharply in the main Nutomonas subclade from all marine species, being exceptionally short compared with earlier-diverging marine clades. Nutomonas longa is very distant but Nutomonas howeae subsp. lacustris differs from Nutomonas (Planomonas) howeae and limna (new combinations) mainly by ITS2 compensatory and/or hemi-compensatory mutations.
    Ancyromonas indica, atlantica, and kenti are genetically more distinct from Ancyromonas sigmoides (=Planomonas mylnikovi). The first soil planomonad (new Nutomonas limna subspecies) was isolated.

  • POSTnote: Biodiversity Offsetting

    • UK Parliamentary Office of Science & Technology
    • 2011

    Given growing recognition of the importance of biodiversity, all sectors are looking for ways to mitigate the environmental costs of development activity. Biodiversity offsetting refers to market-based schemes designed to compensate for losses of biodiversity due to development projects. This POSTnote summarises biodiversity offsetting and examines opportunities and risks of offsets within a UK context.

  • The novel marine gliding zooflagellate genus Mantamonas (Mantamonadida ord. n.: Apusozoa)

    • Protist
    • 2011
    Authors: Edvard Glücksman, Libby Snell, Cédric Berney, Ema E. Chao, David Bass, Thomas Cavalier-Smith

    Mantamonasis a novel genus of marine gliding zooflagellates probably related to apusomonad and planomonad Apusozoa. Using phase and differential interference contrast microscopy we describe the type speciesMantamonas plasticasp. n. from coastal sediment in Cumbria, England. Cells are ∼5 μm long, ∼5 μm wide, asymmetric, flattened, biciliate, and somewhat plastic. The posterior cilium, on which they glide smoothly over the substratum, is long and highly acronematic. The much thinner, shorter, and almost immobile anterior cilium points forward to the cell's left. These morphological and behavioural traits suggest thatMantamonasis a member of the protozoan phylum Apusozoa. Analyses of 18S and 28S rRNA gene sequences ofMantamonas plasticaand a second genetically very different marine species from coastal sediment in Tanzania showMantamonasas a robustly monophyletic clade, that is very divergent from all other eukaryotes. 18S rRNA trees mostly placeMantamonaswithin unikonts (opisthokonts, Apusozoa, and Amoebozoa) but its precise position varies with phylogenetic algorithm and/or taxon and nucleotide position sampling; it may group equally weakly as sister to Planomonadida, Apusomonadida orBreviata. On 28S rRNA and joint 18/28S rRNA phylogenies (including 11 other newly obtained apusozoan/amoebozoan 28S rRNA sequences) it consistently strongly groups with Apusomonadida (Apusozoa).

  • Closely related protist strains have different grazing impacts on natural bacterial communities

    • Environmental Microbiology
    • 2010
    Authors: Edvard Glücksman, Thomas Bell, Robert I. Griffiths, David Bass

    Heterotrophic protists are abundant in most environments and exert a strong top-down control on bacterial communities. However, little is known about how selective most protists are with respect to their bacterial prey. We conducted feeding trials using cercomonad and glissomonad Cercozoa by assaying them on a standardized, diverse bacterial community washed from beech leaf litter. For each of the nine protist strains assayed here, we measured several phenotypic traits (cell volume, speed, plasticity and protist cell density) that we anticipated would be important for their feeding ecology. We also estimated the genetic relatedness of the strains based on the 18S rRNA gene. We found that the nine protist strains had significantly different impacts on both the abundance and the composition of the bacterial communities. Both the phylogenetic distance between protist strains and differences in protist strain traits were important in explaining variation in the bacterial communities. Of the morphological traits that we investigated, protist cell volume and morphological plasticity (the extent to which cells showed amoeboid cell shape flexibility) were most important in determining bacterial community composition. The results demonstrate that closely related and morphologically similar protist species can have different impacts on their prey base.

  • Chapter 2: Assessing the vulnerability of species in Europe and the biogeographic regions to climate change

    • BRANCH project final report, Natural England, UK
    • 2007
    Authors: Edvard Glücksman, Pamela Berry, Claire Thomson, Jesse O’Hanley

    In spite of the fact that climate change impacts on species have been shown to vary widely across different taxa and geographical regions, little work has been done to develop simple quantitative measures with which to compare species and regional vulnerabilities to climate change. This study seeks to address this issue by presenting vulnerability indices that capture both a species’ sensitivity and capacity to adapt to climate change for Europe and for the bioregions (Figure 2.1). Sensitivity, which measures the relative change between current and future climate space, is determined based on the output of the bioclimatic envelope model, SPECIES. Key sensitivity indicators include gained climate space, lost climate space, the overlap between present and future climate space, and the area of future climate space relative to the total study area. Adaptability is assumed to be a function of the extent of new climate space, as this indicates the limit of a species’ potential future distribution. Two extreme cases are considered: either (1) a species makes full use of its new climate space via long distance dispersal, translocation, the creation of habitat corridors, etc., that is perfect adaptation or (2) none of the new climate space is utilised due to limited dispersal capabilities and the absence of any planned intervention strategies, no adaptation. Vulnerability is calculated based on a scoring system for sensitivity and adaptability for a range of terrestrial species, some of which are particularly associated with coastal habitats.

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