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BioIsoK SIGNED

Mechanisms of K stable isotope fractionation in vertebrates and significance to their energy metabolism

Total Cost €

0

EC-Contrib. €

0

Partnership

0

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 BioIsoK project word cloud

Explore the words cloud of the BioIsoK project. It provides you a very rough idea of what is the project "BioIsoK" about.

constitute    modern    driving    potassium    otherwise    metabolic    cu    mass    metals    organisms    intensity    first    ms    inherent    hindrances    vertebrate    ca    fisher    democratization    dependent    unprecedented    energy    inaccessible    compositions    reg    fe    prototype    itself    biodiversity    mechanisms    rates    body    classes    metabolism    traits    phylogenetic    tissues    inductively    principally    unexplored    perspectives    behavioral    reaction    dynamics    fairly    unraveling    mg    mc    opened    spectrometry    technologies    later    ratios    cycling    precious    icp    origins    ecosystems    functions    coupled    metal    physiological    turned    collector    varying    zn    isotopes    extinct    tim    vertebrates    group    spectrometers    notably    biological    evolution    ecological    species    assets    thermo    fossil    collision    isotope    cell    plasma    advent    elliott    bioessential    reared    reconstruction    proteus    class    apprehending    thermophysiology    natural    stable   

Project "BioIsoK" data sheet

The following table provides information about the project.

Coordinator
UNIVERSITY OF BRISTOL 

Organization address
address: BEACON HOUSE QUEENS ROAD
city: BRISTOL
postcode: BS8 1QU
website: www.bristol.ac.uk

contact info
title: n.a.
name: n.a.
surname: n.a.
function: n.a.
email: n.a.
telephone: n.a.
fax: n.a.

 Coordinator Country United Kingdom [UK]
 Total cost 183˙454 €
 EC max contribution 183˙454 € (100%)
 Programme 1. H2020-EU.1.3.2. (Nurturing excellence by means of cross-border and cross-sector mobility)
 Code Call H2020-MSCA-IF-2017
 Funding Scheme MSCA-IF-EF-ST
 Starting year 2018
 Duration (year-month-day) from 2018-10-01   to  2020-09-30

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    UNIVERSITY OF BRISTOL UK (BRISTOL) coordinator 183˙454.00

Map

 Project objective

The reconstruction of physiological and ecological traits of extinct organisms is crucial for apprehending the dynamics of the evolution of species and ecosystems as well as the origins of modern biodiversity. The recent advent of the use of natural stable isotopes of bioessential metals is principally related to the democratization of multi-collector inductively coupled plasma mass spectrometers (MC-ICP-MS). These isotope systems (Mg, Ca, Cu, Fe or Zn) opened up unprecedented perspectives for the study of their cycling in past and present vertebrate organisms and turned out to be precious assets for the unraveling of otherwise inaccessible biological features of fossil organisms, being ecological, behavioral or physiological characteristics. Potassium (K) is a bioessential metal in all vertebrates, where its cycling intensity is notably dependent on their metabolic rates, the later varying itself with thermophysiology from a phylogenetic class to another or with body mass within a given class. Due to its crucial biological functions as well as the observed significant effects of biological processes on its isotope ratios, K isotopes constitute a highly promising novel isotope system for the study of vertebrate metabolism. However, the K stable isotope compositions of vertebrate tissues are currently fairly unexplored, notably due to major technical hindrances, inherent to the existing mass spectrometry technologies. This project aims first to develop a reliable method of K stable isotope analysis using the state-of-the-art “Proteus” prototype MC-ICP-MS implemented with the collision-reaction cell technology and developed by Tim Elliott group and Thermo Fisher®. This method will then be used for analysis of tissues from vertebrates of various classes reared in controlled conditions. This will allow identifying the main mechanisms driving the isotope compositions of vertebrate tissues and assess their potential for the study of vertebrates energy metabolism.

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