Environomics: Taking the pulse on the marine environment

Environomics:
Taking the pulse on the marine
environment
[email protected]
Key Challenges for Environmental
Monitoring Programs
Samples:
-High frequency
-High spatial
resolution
Analysis by
highly trained
taxonomists
Bottleneck!!
Classical environmental monitoring
Schander and Willassen 2005
Key Challenges for Environmental
Monitoring Programs
Samples:
-High frequency
-High spatial
resolution
Analysis by
highly trained
taxonomists
Bottleneck!!
Ideally;
- All species.
- At all times.
- Everywhere.
How do we attain an
accurate ”enough”
characterization of the
marine environment?
”omics”-Technologies
- Genomics
- Epigenomics
- Transcriptomics
- Proteomics
- Metabolomics
Environomics
(Meta-”omics”)
-Who is there? (Meta-genomics)
-What is their potential? (Meta-genomics)
-What are their state? (Meta-transcriptomics and Meta-proteomics)
-How do they influence each other? (Meta-metabolomics)
How an anthropogenic stressor influence the living
marine resourses?
Phylogenetic microarrays and high-throughput sequencing:
A new tool for biodiversity assessment in Northern Norway
Havet og Kysten
Objectives
Our primary objective is to improve the resolution of current environmental monitoring programs
(EMP). Towards this objective we aim to develop and evaluate the potential of using genomic-era
technology (Environomics). Specifically, we aim to conduct:
1. Metagenome sequencing for biodiversity of current monitoring stations to evaluate the environomic
approach.
2. Development and evaluation of microarray technology for species detection for high throughput
biodiversity monitoring (phylochip).
3. Set standards for the coupling between traditional morphology based taxonomy and modern
genomic-era technology.
Biodiversity (”meta”-genomics)
Sampling sites
Universal primers w. site specific tag
5´
Divergent
sequence
site 1
site 2
site 3
All sites are sequenced simultaneously by 454 pyrosequencing
GATCGAAGATCGAGGTAGTGACGAAAAATAACAATACAAGACTCTTCCGAGGCCTTGTAATTGGAATGAGTA
CGTTCCCGAGGATCTATTGGAGGGCAAGTCTGGTGCCAGCAGCCGCGGTAATTCCAGCTCCAATAGCGTAGC
GTTGTGGTTAAAAAGCTCGTAGTTGGATTTCGGCGGGTATTGGTCGGTTTGAATAGCTTCAACACTGACTTT
species sequence
site tag
Why eukaryotic microorganisms?
Meiofaunal versus micro-organism approach
Meiofaunal approach
(12% microorganisms)
Microorganism approach
(79% microorganisms)
Fungi
Porifera
Rhizaria
Dinoflagellates
Ciliates
Apicomplexa
Diatoms
Chlorophyta
Plathyhelminthes
Annelida
Nematoda
Arthropoda
Creer et al., 2010
Separation of different marine sediments
Clay
Oligohymenophorea
Litostomatea
Dinophyceae
ascomycota
Coscinodiscophyceae
Polychaeta
Fine sand
Demospongiae
Karyorelictea
Turbellaria
Conoidasina
Ichthyosporea
Chromadorea
Medium sand
Laberinthulomycetes
Coscinodiscophyceae
Ostracoda
Phyllopharyngea
Vannellidae
Maxillopoda
Coarse sand
Oligohymenophorea
Chlorarachniophyceae
Euamoebida
Anthozoa
Haptophyceae
Chrysophyceae
Trebouxiophyceae
Mediophyceae
Bacillariophyceae
Imbricatea
udef
Principal Component analysis of 4 sediments
Medium and Medium
coarse sand
sand
0,5
Coarse sand
B2
B1
B3
C1
Factor 2 : 12,11%
C3
Fine sand
C2
0,0
A3
A1
A2
Clay
-0,5
D2
D3
D1
clay and fine sand
-1,0
-0,5
Factor 1 : 50,94%
Phylogenetic microarrays
http://www.mbari.org/ESP/espworks.htm
Capitella capitata
Capitella
Capitella
Capitellidae
Capitellida
Scolecida
Polycheata
Annelida
5`
Protostomia
Coelamata
Metazoa
18S rDNA gene
3`
Key Challenges for Environmental
Monitoring Programs
Samples:
Samples:
-High frequency
-High frequency
-High spatial
resolution
-High spatial
resolution
Analysis by
highly trained
taxonomists
Bottleneck!!
High throughput analysis by
Environomics
No Bottleneck!!
Thank you!
- Katrine Lekang
- Kenan Hadziavdic
- Katrine Sandnes Skaar
- Eric Thompson
- Anders Lantzen
- Inge Jonassen
- Marc Frischer
- Christoffer Schander
- Christian Collin-Hanssen
-Seksjon for anvendt
miljøforskning
-Den Norske Veritas