MERG - Universitetet i Oslo
MERG - Universitetet i Oslo
MERG - Universitetet i Oslo
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merg<br />
info<br />
NEW KNOWLEDGE<br />
by CrOssiNG<br />
DisCipLiNary<br />
barriErs<br />
Report for 2011 and plans for 2012<br />
Our main goal is to<br />
achieve status as a<br />
excellent research<br />
environment at UiO<br />
within 2012<br />
3 • 2012<br />
<strong>MERG</strong> is an<br />
effective arena for a<br />
good working environment<br />
and innovative<br />
research and<br />
teaching.
Index<br />
2nd norwegian Microbiology Meeting (noMi-11)<br />
The NoMi-11 meeting was organized on behalf of the MicroMatNat network.<br />
The second meeting took lace 14.-16. Sep, Hemsedal. It aimed to gather junior<br />
scientists, post doctors, and PhD students working in Norwegian institutions<br />
and companies in the area of microbial biology. The goal of the NoMi-11<br />
meeting was to create a fruitful environment for young scientists to discuss<br />
and interact scientifically with each other. The organising committee was lead<br />
by Thomas Haverkamp<br />
GOals and VIsIOns fOR <strong>MERG</strong> 3<br />
aCTIOn plan fOR 2012 4<br />
MajOR aChIEVEMEnTs In 2011 6<br />
<strong>MERG</strong> REsEaRCh pROjECTs 8<br />
InfTRasTRUCTURE IMpROVEMEnTs 2012 9<br />
BUdGET 10<br />
appEndIx 1: REsEaRCh pROjECTs<br />
appEndIx 2: jIppI REpORT
Goals and Visions for <strong>MERG</strong><br />
Visions<br />
Research<br />
<strong>MERG</strong> is in the frontline of the international research<br />
within microbial ecology and evolutionary biology.<br />
<strong>MERG</strong> is a natural partner in Norwegian and European<br />
research projects and networks.<br />
Service and Communication<br />
<strong>MERG</strong> is a national service centre in bioinformatics and<br />
microbiology laboratories (includes collection, culturing,<br />
storage and training).<br />
<strong>MERG</strong> excels in communicating competence and popularizing<br />
for the public.<br />
bio9905 - bioinforMatics for MetagenoMics and enViron-<br />
Mental sequencing<br />
<strong>MERG</strong> in collaboration with Norwegian Sequencing Centre and ForBio arranged<br />
a 5 days intensive course in April. The course had both national and<br />
international speakers, including Karl Inne Ugland, Thomas Haverkamp, Lex<br />
Nederbragt, Anders Lanzén, Ramiro Logares, Christopher Quince, Anders<br />
Nielsen, Surendra Kumar and Håvard Kauserud (course organizer). The<br />
course received funding from Department of Biology, MLS uio and ForBio.<br />
Our main goal is to achieve status as<br />
an excellent research environment<br />
at UiO within 2012.<br />
Teaching<br />
<strong>MERG</strong> is a place for excellent teaching at the masters<br />
and PhD-level by the integration of research and teaching.<br />
<strong>MERG</strong> is the preferred national source of knowledge on<br />
microbial ecology and evolutionary biology.<br />
Organization<br />
<strong>MERG</strong> is an effective and open organization and an<br />
arena for a good working environment, as well as for innovative<br />
research and teaching.
action plan for 2012<br />
JiPPi & annual rePorts<br />
• Jippi on UiO nettskjema<br />
• Jippi goal - 2012<br />
• Main responsible: Kathrine<br />
• <strong>MERG</strong> annual report January 2013<br />
• Responsible: Kamran<br />
hMs focus<br />
• SOP and risk assessment<br />
• Working environment<br />
• Main responsible: Kathrine<br />
infrastructure<br />
<strong>MERG</strong> web-pages<br />
• Simplify the webpages<br />
• Improve the people’s homepages<br />
• Internal pages for each project<br />
• Protist2012 webpages<br />
• Main responsible: Kathrine<br />
Merg is the local host for the conference Protist2012<br />
Protist2012 will cover key topics in eukaryote microbiology. Latest<br />
news in the field of genomics, biodiversity, cell biology and<br />
technological innovations will presented. Protist2012 will take<br />
place 29 July - 3 August 2012 at Georg Sverdrups hus at Blindern<br />
campus. The organizing committee is Anders Krabberød, Rakel Blaalid,<br />
Hanne Ballestad, Kathrine Schou and Kamran Shalchian-Tabrizi.<br />
For more information: http://www.protist2012.org<br />
The action plan for 2012 is developed<br />
through an evaluation seminar<br />
in november 2011 where all participants<br />
contributed. Under each focus<br />
area the actions are describes with<br />
deliverables and responsibilities.<br />
here are all the main actions described.<br />
Bioinformatics and computational infrastructures<br />
• Improve computing / bioinformatics infrastructure.<br />
• Databases for the labs, Bioportal, programs for sequence<br />
analyses and imaging, statistical programs<br />
• Main responsible: Kathrine<br />
Wet lab infrastructures<br />
• Promote Microlab for new user groups<br />
• Manage the new Microlab infrastructure<br />
• Main responsible: Kathrine<br />
Technicians<br />
• Apply for funding for technicians and running costs<br />
• Main responsible: Kathrine
VisualiZation of Merg<br />
Administrative<br />
• UiO reporting systems<br />
• Define <strong>MERG</strong> on CRISTIN<br />
• Main responsible: Kathrine<br />
External communication<br />
• Promote <strong>MERG</strong> in regular courses and in presentations<br />
– develop appropriate PP slides<br />
• Active use of the <strong>MERG</strong> profile: ppt, NEWS, poster,<br />
corridors, doors<br />
• 4 articles on forskning.no, in Apollon (UiO magazine)<br />
or in National newspapers<br />
• Main responsible: All<br />
Meetings & conferences<br />
Protist2012:<br />
• Planning the conference: program, dates, localities<br />
and all necessary information on specific web-page<br />
• Establish E-pay and email-lists<br />
• Main responsible: Kamran<br />
inforMation, education & celebration<br />
Information<br />
• MEWS – <strong>MERG</strong> News<br />
• Organize Tuesday seminars every Tuesday January<br />
to May and September to December<br />
• Main responsible: Kamran<br />
Celebration<br />
• Champagne celebration last Friday of every month<br />
• Jippi party last Friday in November<br />
• Main responsible: Kamran<br />
Courses<br />
• Microscopy, fieldwork and culturing<br />
• Main responsible: Dag K<br />
Journal clubs<br />
• Develop new journal club course at<br />
Department of Biology<br />
• Main responsible: Håvard<br />
<strong>MERG</strong> marked<br />
• Establish marketing place with <strong>MERG</strong> information in<br />
<strong>MERG</strong> area<br />
• Main responsible: Kathrine<br />
Merg eVents<br />
<strong>MERG</strong> Seminars take place every Tuesday in room 4213 at 12:15. Presentation<br />
of project and results will be followed by a discussion.<br />
<strong>MERG</strong> Journal clubs take place every second Wednesday in room 4213 at<br />
13:15<br />
For more events in 2012 see:<br />
http://www.mn.uio.no/bio/english/research/groups/merg/Events/<br />
iMProVe research ProPosals<br />
• If the CoE grant proposal reach the final write CoE<br />
grant proposal together with microbiology research<br />
groups at UiO<br />
• Improve dissemination, ethics and gender issues in<br />
all grant proposals<br />
• Initiate actions to improve chances for achieve EU<br />
grants, focus on Marie Currie grants<br />
• Main responsible: Kamran<br />
recruitMent<br />
China and India – Norway programs<br />
• Communicate <strong>MERG</strong> to RCN responsible for China<br />
and India – Norway programs – to recruit people to<br />
<strong>MERG</strong>.<br />
• Main responsible: Kamran<br />
<strong>MERG</strong> open day<br />
• <strong>MERG</strong> open day – presentation of activity, demonstration<br />
of equipment and projects for master students<br />
• Main responsible: Kamran<br />
cooPeration across Merg<br />
• Arrange two annual workshops/seminars on specific<br />
themes<br />
• Establish “interest groups”<br />
• Common grant applications – establish teams that<br />
write proposals<br />
• Main responsible: All<br />
disseMination, ethics & gender issues<br />
• Initiate collaboration with the School Laboratory in<br />
Biology, UiO for dissemination of results<br />
• Apply for gender equality grants from UiO<br />
• Implement ethics standards recommended by “Forskningsetiske<br />
kommitteer<br />
• Define <strong>MERG</strong> specific ethic guideline and statement<br />
• Main responsible: Kamran<br />
integration of technicians<br />
• Improve the technicians involvement in <strong>MERG</strong> research<br />
and teaching<br />
• Main responsible: Kathrine
Microlab<br />
<strong>MERG</strong> has established a new infrastructure for microbiology research at the<br />
University of <strong>Oslo</strong>, Department of Biology. Access will be granted to staff,<br />
guests and students at UiO working with microorganism cultures and/or eukaryotic<br />
cells, as well as ”field” material. For access and questions contact<br />
Cecilie Mathiesen and Kathrine Schou.<br />
More about the Microlab, see:<br />
http://www.mn.uio.no/bio/english/research/groups/merg/<br />
Major achievements in 2011<br />
Publications<br />
In 2011 <strong>MERG</strong> published 4 more articles than in 2010,<br />
and is the most productive year since the group was<br />
established. Altogether 31 articles were published.<br />
Inter-disciplinary publications<br />
Several of our papers have a clear cross-disciplinary<br />
profile where different types of expertise have been<br />
combined to achieve common goals. Two of these are<br />
presented here. The article by Kumar et al. presents a<br />
new bioinformatics pipeline named CLOTU dedicated<br />
to processing of DNA sequences generated by the 454<br />
technology. In this work expertise in microbiology, informatics<br />
and statistics worked together.<br />
The other paper by Krabberød et al. investigates the<br />
phylogeny of a group of unculturable group of eukaryotes<br />
by applying fieldwork, whole genome amplification<br />
<strong>MERG</strong>’s main goal is to achieve a<br />
status as an excellent research environment<br />
within 2012. We reached<br />
this goal in 2011 by participating on<br />
a proposal for a Centre for Integrative<br />
Microbiology, which received<br />
the score Excellent by an international<br />
review panel. The finalists<br />
will be announces in May.<br />
and phylogenetic analyses. To accomplish the work, experts<br />
in biochemistry, micropaleontology, bioinformatics<br />
and evolutionary biology where brought together.<br />
• Krabberød, Anders Kristian; Bråte, Jon; Dolven,<br />
Jane Karine Lønne; Ose, Randi Frida; Klaveness,<br />
Dag; Kristensen, Tom; Bjørklund, Kjell Rasmus et<br />
al. (2011). Radiolaria Divided into Polycystina and<br />
Spasmaria in Combined 18S and 28S rDNA Phylogeny<br />
. PLoS ONE. doi: 10.1371<br />
• Kumar, Surendra; Carlsen, Tor; Mevik, Bjørn-Helge;<br />
Enger, Pål; Blaalid, Rakel; Shalchian-Tabrizi, Kamran<br />
& Kauserud, Håvard (2011). CLOTU: An online<br />
pipeline for processing and clustering of 454 amplicon<br />
reads into OTUs followed by taxonomic annotation<br />
. BMC Bioinformatics. doi: 10.1186/1471-2105-<br />
12-182
Impact factor<br />
The two papers published in 2011 with highest impact<br />
factor (IF) were:<br />
• Buntgen U, Kauserud H, Egli S. 2011. Linking climate<br />
variability to mushroom productivity and phenology.<br />
Frontiers in Ecology and the Environment, in press<br />
(IF: 8.8)<br />
• Eastwood et al. 2011. The Plant Cell Wall‚ Decomposing<br />
Machinery Underlies the Functional Diversity<br />
of Forest Fungi. Science 333, 762 (IF: 31)<br />
All 2011 publications see the appendix 2.<br />
Highly cited papers<br />
In 2011 two articles were on the top cited articles in two<br />
international peer reviewed journals. Burki et al. 2008<br />
and 2009 are currently at top cited list in Biology Letters<br />
Genome Biology and Evolution.<br />
• Burki, F; Shalchian-Tabrizi, Kamran & Pawlowski, J<br />
(2008). Phylogenomics reveals a new ‘megagroup’<br />
including most photosynthetic eukaryotes. Biology<br />
Letters. ISSN 1744-9561. 4, s 366- 369 . doi:<br />
10.1098/rsbl.2008.0224<br />
• Burki, Fabien; Inagaki, Yuji; Bråte, Jon; Archibald,<br />
John M; Keeling, Patrick J; Cavalier-Smith, Thomas;<br />
Sakaguchi, Miako et al. (2009). Large-Scale Phylogenomic<br />
Analyses Reveal That Two Enigmatic Protist<br />
Lineages, Telonemia and Centroheliozoa, Are Related<br />
to Photosynthetic Chromalveolates. Genome<br />
Biology and Evolution. ISSN 1759-6653. 1(1), s<br />
231-238 . doi: 10.1093/gbe/evp022<br />
research and serVice aPPlications<br />
In 2011 <strong>MERG</strong> staff took part in 11 larger grant applications<br />
to national and international grant offices. These<br />
are the following highlight:<br />
Centre of Excellence (CoE)<br />
<strong>MERG</strong> applied for a Centre of Excellence named Centre<br />
for Integrative Microbiology (CIM) together with three<br />
other microbial biology research groups at the University<br />
of <strong>Oslo</strong> (Glyconor, LaMDa, <strong>MERG</strong> and Tone Tønjumgroup)<br />
and external collaborators to maximize the potential<br />
synergies. The assessment gave an overall score<br />
excellent. The outcome of the prequalification round will<br />
be announced in May 2012.<br />
ERC starting grant application<br />
In November 2011 Håvard Kauserud submitted an ERC<br />
starting grant application to the European Research<br />
Council entitled “Linking microbial communities in boreal<br />
forest soils to plant diversity and productivity – a<br />
metagenomics approach”. The goal of this project is to<br />
make fundamental progress in the understanding of the<br />
community ecology of microorganisms in boreal forest<br />
soils and how they are organized spatiotemporally. The<br />
diversity, composition and activity of microbial communities<br />
will be related to the diversity and productivity of<br />
co-occurring plants.<br />
Grants from Research Council of Norway and UiO<br />
Project leader Dag Klaveness, got funded the project:<br />
“X-cell parasites: an emerging threat to marine fish”. This<br />
project is a collaboration with Kamran Shalchian-Tabrizi,<br />
Mark Freeman, University of Malaya, David Bass, Natural<br />
History Museum, London and Håkon Hansen, Norwegian<br />
Veterinary Institute, Norway.<br />
The project ”Regulatory RNA and the origin of animal<br />
multicellularity” got funded by an UiO PhD position (Ralf<br />
Neumann) and a, postdoc position to Jon Bråte. The<br />
projects aims to investigate whether the RNAi machinery<br />
was lost from the genomes of single-celled ancestors<br />
of animals multiple times and if the miRNA pathway<br />
evolved independently in animals with respect to other<br />
eukaryotic supergroups.<br />
All scientific project see the appendix 1<br />
high PerforMance coMPuting<br />
The capabilities of the Bioportal will be expanded to meet<br />
the Life Science users’ computational needs. The major<br />
objective with the requested project from NOTUR is to<br />
implement the Galaxy infrastructure at the computational<br />
resources at UiO and develop this system to handle<br />
jobs from the Bioportal. Porting jobs from the Bioportal<br />
to the Galaxy system will have several advantages. This<br />
project is a collaboration between BIO, USIT and CLSi.<br />
eValuation<br />
In the BIO-fag evaluation from 2010 the research program<br />
<strong>MERG</strong> got a good – very good score. The BIO-fag<br />
evaluation is based on achievement from 2000-2009.<br />
infrastructure<br />
The Microlab facility at Department of Biology was<br />
opened in December 2011. The facility is designed and<br />
managed by <strong>MERG</strong>. The Microlab is established for<br />
storage and growth of microbial cells of prokaryotes<br />
and eukaryotes species a well as virus, and other kinds<br />
of cell tissues from multicellular organisms such as animals<br />
and plant. The Microlab will be used for research<br />
on algea, fungi, protozoa, several bacteria strains and<br />
salmon cells. More about this infrastructure see <strong>MERG</strong><br />
web-pages.<br />
new web-Pages<br />
New <strong>MERG</strong> web pages have been made - see<br />
http://www.merg.uio.no<br />
new coMMunication Profile for Merg<br />
New profile including power-points, posters, newsletters,<br />
colour pallet and elements was ready September<br />
2011. This is intended for <strong>MERG</strong> internal and external<br />
use.<br />
all achieVeMent 2011 in the JiPPi rePort<br />
Activities in <strong>MERG</strong> has been reported in the JIPPI, more<br />
information about JIPPI and the activities in <strong>MERG</strong> 2011,<br />
see appendix 2.
write-it-right<br />
In January Anke Stuken invited Gadi Rothenberg and Christopher Lowe to<br />
UiO to course 40 PhD students, postdocs, and researchers. For a successful<br />
career in research you must get your work published, read and cited. In<br />
our Write it Right (WiR) workshops we learnt how to: Write clear technical<br />
English, Structure our article effectively, Enhance titles and graphics to make<br />
an impact<br />
<strong>MERG</strong> research projects<br />
The <strong>MERG</strong> on going research project<br />
covers a wide range of areas<br />
in microbial ecology and evolution.<br />
here is a overview of the title of<br />
the projects. further details of the<br />
research content and the participating<br />
teams are<br />
described on <strong>MERG</strong> web pages.<br />
• Regulatory RNA and the origin of animal multicellularity.<br />
• X-cell parasites: an emerging threat to marine fish.<br />
• Population diversification and horizontal gene transfer processes in freshwater cyanobacteria: genomic and<br />
ecological perspectives.<br />
• Saxitoxin biosynthesis and genomics in organisms from two kingdoms - horizontal gene transfer or parallel<br />
evolution?<br />
• Biodiversity of marine eukaryotes (BioMarKs).<br />
• Phylogenomic and single cell whole genome amplification of Radiolaria.<br />
• Bioinformatics applications for evolutionary and ecologically high throughput sequence analysis.<br />
• A molecular phylogeny of the brown-spored agarics (Basidiomycota).<br />
• Endophytic fungi in boreal forest bryophytes.<br />
• Population genetics and phylogeography of Serpula lacrymans.<br />
• Comparative genomics of Serpula spp.<br />
• Microbial ecology of mycorrhizal symbiosis.<br />
• Fungi and climate change.<br />
• Ectomycorrhiza on Salix repens in coastal ecosystems on Lista peninsula, Vest-Agder, SW Norway.<br />
• Origin of animals and plants.<br />
• Evolutionary diversification and functional genomic studies of the Collodictyonidae.<br />
• Hydrurus foetidus, a large freshwater representative of the Chromalveolate (SAR?) clade.<br />
• Habitat fragmentation and pathways to extinction in dead-wood dependent fungi.<br />
• Advanced monitoring of the introduced crayfish plague (Aphanomyces astaci) for improved management of<br />
endangered freshwater crayfish.<br />
• High throughput sequencing of deep sea metagenomes.<br />
• Alkaloid profiles in Claviceps purpurea - relationships between chemotype, genotype, host and habitat.
adVanced equiPMent aPPlication<br />
The total figure announced for new applications of equipment and infrastructure<br />
is NOK 22,828,000. Applicable funding is categorized into advanced scientific<br />
equipment, scientific databases and collections and eInfrastructure,<br />
and costing at least NOK 1 million. Suitable coordinated applications across<br />
the university will be favoured. Grants will be made on the bases of the longterm<br />
priorities for academic and research activities. Our candidates are: BI-<br />
OLOG and Influx flow (see illustrations). Deadline for application is 1.March.<br />
Infrastructure improvement 2012<br />
At present the Bioportal, a web-based front-end to the<br />
computational resource Titan at the University of <strong>Oslo</strong><br />
(UiO), is a highly successful method for accessing the<br />
resource for many researchers in the field of life science.<br />
The primary goal with the Bioportal has been to reduce<br />
the barriers for users to explore the HPC resources. The<br />
success of the Bioportal is largely due to the simplified<br />
user interface that enables non-programmers access to<br />
advanced computational tools in their research. Close<br />
to 3 million CPU hours were consumed through the Bioportal<br />
during the last allocation period (2010.2). The<br />
usage prognosis for the present period is the same, limited<br />
only by the present allocation. As the demand for<br />
simplified and user-centric interfaces to computational<br />
resources are increasing, so is the demand for a wider<br />
range of applications and tools presented through these<br />
interfaces.<br />
Bioportal is a web-based bioinformatics<br />
service at UiO, which is initiated by<br />
<strong>MERG</strong> participants.<br />
Bioportal is the most used bio-informatics service in norway. In 2012 we<br />
will implement Galaxy as an infrastructure middleware.<br />
obJectiVes of the ProJect<br />
The major objective with the requested project from<br />
NOTUR is to implement the Galaxy infrastructure at the<br />
computational resources at UiO and develop this system<br />
to handle jobs from the Bioportal.<br />
the teaM<br />
Kamran Shalchian-Tabrizi (BIO), Hans A Eide (USIT),<br />
Bjørn-Helge Mevik (USIT), Katerina Michalickova (USIT),
Merg<br />
Budget<br />
Microbial eVolution research grouP<br />
<strong>MERG</strong> works strategically to improve our research by creating synergies<br />
across the group and with external collaborators. The core of our research<br />
area is microbial ecology and evolution. We address basic theoretical and<br />
methodological questions for a broad group of microorganisms, and aim to<br />
apply this knowledge to solve challenges within health, climate, environment,<br />
energy and food production. Our research and teaching is inter-disciplinary<br />
and aim at creating synergies across wide range of disciplines.<br />
for 2012 <strong>MERG</strong> is anticipated to get a base funding of approximately<br />
416.000 nOK for running cost from the department of Biology. This year<br />
we will focus on upgrading the areas outside room 4212 as a “<strong>MERG</strong><br />
market”. We will continue with champagne celebrations and the jIppI party<br />
the last friday in november. 40 000 is allocated travel support.<br />
Microbial Evolution Research Group (<strong>MERG</strong>), www.merg.uio.no<br />
Mail address P.O box 1066 Blindern 0316 <strong>Oslo</strong> Norway<br />
Contact person: Kamran Shalcian-Tabrizi, kamran@bio.uio.no<br />
traVel suPPort<br />
Support up to 3000 NOK for traveling to conferences,<br />
courses and research stay abroad will be transerred to<br />
<strong>MERG</strong> participants based on JIPPI registration at the<br />
end of the year.<br />
Merg Maked Place<br />
The area outside room 4212 will be renovated and furnished<br />
during 2012. The intention is to improve our visibility<br />
at the department by displaying news, printed articles<br />
and announcements. 30 000 NOK is allocated to<br />
this work.<br />
Microlab<br />
The new labs have opened and needs 50 000 NOK for<br />
simple equipment.<br />
JiPPi celebration<br />
In 2012 we will celebrate the <strong>MERG</strong> activity the last Friday<br />
in November at a restaurant in <strong>Oslo</strong>. 30 000 NOK is<br />
allocated to this event in the budget.<br />
furniture<br />
2012 is the last year we are paying for our office furniture.<br />
We have each of the three last year spent about<br />
140 000 NOK on new kitchen, desks, chairs and shelfs.
<strong>MERG</strong><br />
Annual report 2011<br />
APPENDIX 1: <strong>MERG</strong> Research<br />
Projects 2012<br />
Microbial Evolution Research Group (<strong>MERG</strong>)<br />
Department of Biology<br />
University of <strong>Oslo</strong>
Index<br />
<strong>MERG</strong><br />
In alphabetic order:<br />
A molecular phylogeny of the brown-spored agarics (Basidiomycota) ........ 3<br />
Advanced monitoring of the introduced crayfish plague (Aphanomyces<br />
astaci) for improved management of endangered freshwater crayfish ........ 4<br />
Alkaloid profiles in Claviceps purpurea - relationships between chemotype,<br />
genotype, host and habitat .......................................................................... 5<br />
Biodiversity of marine eukaryotes (BioMarKs) ............................................ 6<br />
Bioinformatics applications for evolutionary and ecologically high<br />
throughput sequence analysis ..................................................................... 7<br />
Comparative genomics of Serpula spp. ........................................................ 8<br />
Ectomycorrhiza on Salix repens in coastal ecosystems on Lista peninsula,<br />
Vest-Agder, SW Norway .............................................................................. 9<br />
Endophytic fungi in boreal forest bryophytes ........................................... 10<br />
Evolutionary diversification and functional genomic studies of the<br />
Collodictyonidae ......................................................................................... 11<br />
Fungal speciation ...................................................................................... 12<br />
Fungi and climate change .......................................................................... 13<br />
Habitat fragmentation and pathways to extinction in dead-wood dependent<br />
fungi .......................................................................................................... 14<br />
High throughput sequencing of deep sea metagenomes ............................ 15<br />
Hydrurus foetidus, a large freshwater representative of the<br />
Chromalveolate (SAR?) clade ..................................................................... 16<br />
Microbial ecology of mycorrhizal symbiosis .............................................. 17<br />
Origin of animals and plants ..................................................................... 18<br />
Phylogenomic and single cell whole genome amplification of Radiolaria .. 19<br />
Population diversification and horizontal gene transfer processes in<br />
freshwater cyanobacteria: genomic and ecological perspectives ............... 20<br />
Population genetics and phylogeography of Serpula lacrymans ................ 21<br />
Saxitoxin biosynthesis and genomics in organisms from two kingdoms -<br />
horizontal gene transfer or parallel evolution? ......................................... 22<br />
Regulatory RNA and the origin of animal multicellularity ........................ 23<br />
X-cell parasites: an emerging threat to marine fish .................................. 24<br />
2
<strong>MERG</strong><br />
A molecular phylogeny of the brown-spored agarics<br />
(Basidiomycota)<br />
Objectives of the project<br />
• Re-analyse the current classifications schemes of the brown-spored agarics and define<br />
monophyletic groups.<br />
• Track and analyse the evolution of various mycorrhizal and saprotrophic life-forms.<br />
• Analyse infrageneric molecular phylogeny in Galerina, and test species boundaries and character<br />
evolution, using a multi-locus phylogenetic approach.<br />
• Analyse infrageneric molecular phylogeny in Cortinarius, and track the evolution of chemical,<br />
morphological and ecological characters in light of the molecular results.<br />
• Perform a critical examination of the G. atkinsoniana and G. marginata species complexes, using a<br />
combination of multi-locus sequencing and AFLP fingerprints.<br />
Galerina marginata, Photo: Klaus Høiland<br />
Project summary<br />
The brown-spored agarics include saprotrophic and mycorrhizal fungi belonging to the families<br />
Bolbitiaceae, Cortinariaceae, Crepidotaceae, and Strophariaceae. The taxonomy is largely based on<br />
morphological and ecological characters, as in most groups of fungi. In this PhD project, our main goal<br />
is to support species and genus level distinction by using DNA sequence data to infer phylogenetic<br />
relatedness and character evolution, and subsequently, to approach a phylogenetic classification of the<br />
brown-spored agarics. Multilocus sequence data sets will be analyzed using parsimony and maximum<br />
likelihood based phylogenetic methods. A special emphasis is put on the genus Galerina, which<br />
includes saprotrophic and bryophilous species producing small, mycenoid and yellow to brownish<br />
basidiocarps.<br />
The team<br />
Øyvind Stensrud (PhD), Trond Schumacher, Håvard Kauserud, Klaus Høiland + external collaborators.
<strong>MERG</strong><br />
Advanced monitoring of the introduced crayfish plague<br />
(Aphanomyces astaci) for improved management of endangered<br />
freshwater crayfish<br />
Objectives of the project<br />
Develop and apply molecular methods for direct monitoring of crayfish plague (CP) in water and<br />
environment in order to 1) explore the ecology and adaptation of Aphanomyces astaci in freshwater<br />
systems and 2) develop rapid, reliable and cost efficient tools for improved management of endangered<br />
freshwater crayfish.<br />
Signal crayfish (left) and noble crayfish (right,)<br />
Photo: David Strand<br />
Sub-goals:<br />
1) Develop an operational real-time PCR for direct and<br />
quantitative monitoring of CP in freshwater and<br />
freshwater environment<br />
2) Compare the levels of CP-infection in signal crayfish<br />
stocks and their freshwater environments<br />
3) Target potential alternate hosts for A. astaci from Nordic<br />
freshwater systems<br />
4) Develop molecular markers for direct monitoring and<br />
epidemiological studies of low- and high virulent CPgenotypes.<br />
5) Determine the distribution of CP-genotypes involved in<br />
previous & present Norwegian outbreaks<br />
Project summary<br />
Aphanomyces astaci is a specialized parasite on North American freshwater crayfish. Accidental<br />
introduction of A. astaci to Europe resulted in the lethal crayfish plague (CP). Later introductions of<br />
North American carrier crayfish to Europe has accelerated CP spread and established constant<br />
infection reservoirs. Due to CP, European freshwater crayfish are endangered, and the crayfish<br />
businesses suffer great economical losses. In Norway, CP is listed as a group A disease, and<br />
introduction of carrier crayfish is prohibited. Several outbreaks of CP have wiped out Norwegian<br />
populations of noble crayfish, and illegally introduced carrier crayfish was recently detected. Growing<br />
evidence indicate that CP may persist longer than previously thought, which complicates re-stocking<br />
activities. In 2005, CP killed reintroduced crayfish stocks in two Norwegian watercourses. Recently, the<br />
Minister of Fisheries and Coastal Affairs asked the competent authorities to develop strategies to<br />
combat CP and signal crayfish in Norway. The major objective of the proposed project is to develop<br />
and apply molecular methods for direct monitoring of A. astaci in water and environment in order to 1)<br />
explore the ecology of A. astaci in freshwater systems and 2) develop rapid, reliable and cost efficient<br />
tools for improved surveillance that will enhance sustainable management and use of freshwater<br />
crayfish. Improved surveillance will include a) early warning of CP infections, b) unveiling illegally<br />
introduced carrier crayfish and c) declare waters free of infection. The project will further explore the<br />
persistence of CP in freshwater habitats and target mechanisms for prolonged survival. Methods for<br />
monitoring high- and low virulent CP-genotypes will be developed in collaboration with active project<br />
partners. The project involves collaboration with reputed national and international institutions that will<br />
ensure needed competence, provide relevant study areas, and enhance research networking<br />
The team<br />
David Strand (PhD), Bente Edvardsen, Dag Klaveness, Trude Vrålstad.<br />
4
<strong>MERG</strong><br />
Alkaloid profiles in Claviceps purpurea - relationships between<br />
chemotype, genotype, host and habitat<br />
Project Summary<br />
The project is about the grass parasitic fungus Claviceps purpurea that produces toxic ergot alkaloids<br />
leading to ergotism and neurological disturbances in mammals. Phylogenetic analyses support three<br />
habitat specific C. purpurea lineages (dry, wet/shady, saline), indicating a habitat driven evolution that<br />
again correspond to unique chemotypes. Recent results suggest that this picture is more complex. The<br />
aim of the project is to test whether the alkaloid profile within a genotype is a function of genotype only,<br />
or also dependent on the host plant. We will further investigate if alkaloid profile variation between<br />
genotypes is larger than the host-plant-determined variation, and if genotypes co-exist within hosts and<br />
habitats.<br />
The team<br />
Mariell Negård (master student). Supervisors: Trude Vrålstad (<strong>MERG</strong>, NVI), Silvio Uhlig & Gunnar<br />
Sundtstøl Eriksen (NVI), and Klaus Høiland (<strong>MERG</strong>)..<br />
5<br />
1. Claviceps purpurea på timotei,<br />
2. Mariell in the field<br />
Photo: Trude Vrålstad
<strong>MERG</strong><br />
Biodiversity of marine eukaryotes (BioMarKs)<br />
Objectives of the project<br />
• Establish a baseline of protist biodiversity in EU coastal waters,<br />
• Measure biodiversity change in marine protist communities facing ocean acidification,<br />
• Evaluate the impact of ballast water and pollution on marine protist biodiversity.<br />
• To significantly enhancing our basic knowledge of eukaryote biodiversity and ecology (Who?<br />
How Many? When? Where? Why?),<br />
Project summary<br />
<strong>MERG</strong> and other research groups at University of <strong>Oslo</strong> participate in the BioMarKs project as one of 8<br />
EU research institutes. More than 30 experts from various biological disciplines, economy and politics<br />
are brought together to address key questions about eukaryote microbial diversity.<br />
BioMarKs integrates expertise in eukaryotic microbial taxonomy and evolution, marine biology and<br />
ecology, genomics and molecular biology, bioinformatics, as well as marine economy and policy, to<br />
assess the taxonomic depth, environmental significance, human health and economical implications of<br />
biodiversity of the unicellular eukaryotes or protists. Exploration of ribosomal rDNA clone libraries over<br />
the last decade has revealed ever-increasing biodiversity in both novel lineages and groups which were<br />
believed to be species-poor. BioMarKs will reassess coastal marine protist biodiversity using massive<br />
454 amplicon sequencing of both rDNA and reverse transcribed rRNA general eukaryote and groupspecific<br />
markers, in order to analyze both diversity and abundance/activity of marine protists at<br />
different taxonomic levels. A suite of physical, chemical, and biological metadata from the same<br />
samples will allow statistical analyses of the ecological forces shaping marine protist biodiversity.<br />
Microscopy analyses, as well as downstream PCR-based and FISH molecular analyses of archive DNA,<br />
RNA, and cellular material (again from the same samples) will allow anchoring of the genetic data into<br />
high quality phenotypic, phylogenetic, and ecological quantitative frameworks.<br />
<strong>MERG</strong> participate in particular on topics related to parasitic organisms and development of<br />
suitable bioinformatics tools for investigation of diversity and abundance of parasitic groups.<br />
The team at UiO:<br />
Wenche Eikrem, Kamran Shalchian-Tabrizi, Tom Andersen, Kjell Bjørklund, Bente Edvardsen.<br />
6<br />
The project has a project<br />
webpage. BioMarKs
<strong>MERG</strong><br />
Bioinformatics applications for evolutionary and ecologically high<br />
throughput sequence analysis<br />
Objectives of the project<br />
To develop bioinformatics tools and subsequent analysis of ever increasing sequences in the context of<br />
ecological and evolutionary microbiology. To apply these newly developed tools on computer<br />
clusters (Bioportal) for ultra high throughput analysis.<br />
Sub goals:<br />
• BLASTGrabber: a user-friendly bioinformatics infrastructure for data mining of sequence database and<br />
downloading aimed for ultra high throughput sequence analysis.<br />
• AIR (Appender, Identifier, Remover): A web based phylogenomic application for efficient creation of<br />
multigene alignments and better assessment of evolutionary rates in sequence alignments.<br />
• CLOTU: A web-based pipeline for clustering and analysis of environmental sequences.<br />
Project summary<br />
This project focuses particularly on solving some of the major obstacles in bioinformatics analyses of large<br />
and complex data in the field of ecological and evolutionary microbiology. The availability of high throughput<br />
sequencing technology at lower cost than previously will certainly cause dramatic increase in the number of<br />
genome sequences in near future. The explosion of genomic sequence information generated immediate<br />
reliance upon ultra high throughput analysis in bioinformatics field. An increase in the amount of large-scale<br />
sequence data does not necessarily lead to an increase in biological knowledge until it is accompanied with new<br />
or improved tools for sequence analysis. The main objective of this project is to develop a user-friendly<br />
bioinformatics infrastructure for data mining of sequence databases and downloading aimed for ultra high<br />
throughput sequence analysis. This infrastructure, which we call BLASTGrabber, will form the basis for<br />
developing one major web-based service freely available to anyone. In addition, this infrastructure will form<br />
the basis for developing two smaller bioinformatics applications in the areas of biodiversity (CLOTU) and<br />
phylogenomics (AIR). All the web-based applications will be made available on the Bioportal at University of<br />
<strong>Oslo</strong>, and it is a goal to contribute to improve research in <strong>MERG</strong> by applying these applications in ongoing<br />
research.<br />
The team<br />
Surendra Kumar (PhD), Kamran Shalchian-Tabrizi, Kjetill S. Jakobsen, Håvard Kauserud.<br />
7
<strong>MERG</strong><br />
Comparative genomics of Serpula spp.<br />
Objectives of the project<br />
• Study the genome evolution among various Serpula lineages.<br />
• Reveal which genomic changes have accompanied the transition from nature to man made habitats.<br />
• Compare genomes features of various geographic populations of S. lacrymans.<br />
• Analyse the genomic changes that have accompanied the ecological transition from saprotrophism<br />
to symbiosis (mycorrhiza) in Serpula.<br />
• Use genome data to study the evolution of mating types (sex chromosome evolution) in Serpula<br />
spp.<br />
Serpula lacrymans<br />
Photo: Sandy Maurice<br />
Project summary<br />
The dry rot fungus Serpula lacrymans is a severe destroyer of wooden building materials in temperate<br />
regions worldwide. It belongs in the Boletales, being relatively closely related to mycorrhiza forming<br />
taxa. It is a brown rot fungus, decaying the cellulose and hemicellulose components of the wood. In<br />
2007, JGI (http://www.jgi.doe.gov/) accepted a proposal to genome sequence S. lacrymans var<br />
lacrymans and its sequence will soon be made publicly available. JGI has also accepted to genome<br />
sequence the closely related S. lacrymans var shastensis using 454 sequencing, where our group is<br />
responsible for providing the genomic DNA. Together with our Swedish collaborators we also plan to<br />
sequence additional genomes of various Serpula lacrymans lineages using Illumina/Solexa sequencing.<br />
The main objectives is to reveal which genomic changes that are associated with the fungus transition<br />
from free-living in nature to becoming the most aggressive indoor decomposer. We also want to extend<br />
the project with genomic comparisons between saprotrophic and mycorrhiza forming Serpula lineages.<br />
The team<br />
Inger Skrede (Post Doc), Sudagar Balasundaram (PhD), Håvard Kauserud + collaborators.<br />
8
<strong>MERG</strong><br />
Ectomycorrhiza on Salix repens in coastal ecosystems on Lista<br />
peninsula, Vest-Agder, SW Norway<br />
Objectives of the project<br />
• Differences between above-ground and below-ground fungal structures.<br />
• The variation of ectomycorrhiza from unestablished to established sand dunes, from rich to poor<br />
soils, from wet to dry soils, and between sand dune ecosystems and heath ecosystems.<br />
• Inocybe_dunensis<br />
Project summary<br />
Creeping Willow Salix repens is an important woody plant in coastal ecosystems such as sand dunes<br />
and heaths. In sand dunes its habitats range from dry to wet and from calcareous, humus-poor to<br />
acidic, humus-rich soils. Its mycorrhizal associations are dual, arbuscular or ectomycorrhizal,<br />
depending on the relative availability of nitrogen and phosphorus. The differences in the habitat<br />
preference of the various ectomycorrhizal morphotypes and arbuscular mycorrhiza suggest that<br />
mycorrhizal diversity contributes to the broad ecological amplitude of S. repens. Moreover, neither<br />
diversity nor abundance of above-ground ectomycorrhizal fungi (assessed as sporocarps) can be used<br />
to assess below-ground ectomycorrhizal diversity or abundance. – No studies employing molecular<br />
detection methods on S. repens mycorrhizae have been performed up to now. Field work has been<br />
performed in various dune and heath systems on the Lista peninsula in April, July and October 2009.<br />
Root tips with ectomycorrhiza have been collected for molecular analyses.<br />
The team<br />
Klaus Høiland, Cecilie Mathiesen, Håvard Kauserud, Tor Carlsen (tentatively team).<br />
9<br />
From left: Fruit bodies<br />
of Inocybe_dunensis and Salix repens<br />
Photo: Klaus Høiland
<strong>MERG</strong><br />
Endophytic fungi in boreal forest bryophytes<br />
Objectives of the project<br />
• Describe the diversity of endophytic fungi in three abundant boreal forest bryophytes across different<br />
habitats and spatial scales, ranging from the single bryophyte shoot up to the global intercontinental<br />
scale.<br />
• Explore how the diversity of fungal endophytes in forest bryophytes is affected by landuse, i.e.<br />
forestry operations.<br />
• Explore how the diversity of endophytes in forest bryophytes is affected by environmental pollution,<br />
i.e. nitrogen deposition and acidification.<br />
• Chemically characterize secondary metabolites produced by fungal endophytes in boreal forest<br />
bryophytes.<br />
• Estimate the role of fungal endophytes in the relationship between bryophytes and herbivores.<br />
Project summary<br />
Fungi that live hidden inside plant tissues, apparently without causing injuries to the host plant appear<br />
to be ubiquitous. These fungi are endophytes and they belong to several fungal taxonomical groups.<br />
While there is a growing appreciation of the ecological importance and human uses of fungal<br />
endophytes in higher plants, remarkably little is known about their host specificity, diversity, and<br />
functional role in bryophytes. In this project, which integrates chemical, microbiological, mycological<br />
and ecological competences, we will study the endophytic fungi and their functional role in three boreal<br />
bryophytes, i.e. Hylocomium splendens, Pleurozium schreberi and Polytrichum commune. You may<br />
wonder, by all right, why we chose to target some tiny bryophytes when there are so many other and<br />
more spectacular plants around? First, these three bryophytes have a circumpolar distribution and they<br />
are extremely abundant in boreal areas. In the boreal biome they occur in all places on land and their<br />
biomass outranges most other boreal organisms. Second, they play an important functional role in<br />
boreal forests, which is the world’s second largest terrestrial biome. The project is funded by NFR (Miljø<br />
2015).<br />
The team<br />
Marie Davey (Post Doc), Lisbeth Thorsvik (scientific assistant), Håvard Kauserud, Mikael Ohlson (UMB)<br />
+ external collaborators.<br />
10<br />
Endophytic fungi<br />
Photo: Marie Davey
<strong>MERG</strong><br />
Evolutionary diversification and functional genomic studies of the<br />
Collodictyonidae<br />
Objectives of the project<br />
- Investigate the molecular phylogeny of a Collodicyonidae species already in culture<br />
- Study the distribution and diversity of possibly related species by means of environmental rDNA<br />
PCR and/or selected genes<br />
- Bring new related organisms in culture for identification of allegedly primitive traits by molecular<br />
methods<br />
- Discuss the relation between these organisms and the concept of the most primitive eukaryote<br />
Project summary<br />
Collodictyon triciliatum Carter 1865 is an amoebo-flagellate originally described from a pond in India. It<br />
is occasionally found in freshwater lakes and rivers, but it is rare and its systematic relationship to other<br />
amoeba and flagellate-like organisms has been uncertain. We have a culture of this organism, isolated<br />
from lake Årungen, and had only done some preliminary light- and electronmicroscopical work on this<br />
organisms. The overall goal of this project is to obtain an understanding of the origin and evolutionary<br />
traits of an allegedly primitive organism, by use of frontline methods now available. In addition, by<br />
employing environmental PCR and recently developed methods using the 454-titanium technology, we<br />
expect to shed light upon the distribution of related organisms in nature, and to obtain a scientifically<br />
founded idea about the evolutionary development and systematic relationship to other organisms. This<br />
may involve a discussion of what are ancestrally primitive eukaryote traits.This investigation leads us<br />
into questions of great general interest.<br />
The team<br />
Sen Zhao (PhD), Jon Bråte (PhD), Klaus Høiland, Kamran Shalchian-Tabrizi, Thomas Rohrlach, Dag<br />
Klaveness.<br />
11<br />
Collodictyon triciliatum<br />
Photo: Dag Klaveness
<strong>MERG</strong><br />
Fungal speciation<br />
Objectives of the project<br />
The main objective in this project is to analyze mechanisms and processes involved during fungal<br />
speciation employing empirical and experimental inferences. More specific aims are to:<br />
• Analyze the geographic component of speciation in fungi (allopatric, parapatric vs. sympatric<br />
speciation).<br />
• Evaluate the importance of ecological differentiation and isolation during fungal speciation.<br />
• Analyze the importance of post-zygotic isolating mechanisms.<br />
• Evaluate the importance of hybridization and reinforcement (Darwinian speciation).<br />
Project summary<br />
Although more than 100.000 fungal species exist, fungi are largely missing<br />
in the speciation debate. Speciation theory is based mainly on research on animals and plants and little<br />
is known whether fungi conform to general models of speciation. Four different boreal/nemoral wooddecay<br />
species complexes (Basidiomycota) will be used as model organisms in this project, selected<br />
because multiple breeding units (intersterility groups) exist within the species complexes, indicating<br />
ongoing or recent speciation. Preliminary data indicates that hybridization and/or introgression occurs<br />
in at least two of the species complexes. One main research topic is to reconstruct speciation<br />
mechanisms in fungi through biogeographical interpretation of phylogenies (phylogeography) based on<br />
multilocus DNA datasets. The ecological component of the speciation process will be studied through<br />
various physiological experiments. Various fitness parameters and ecological characteristics will be<br />
investigated in the divergent allopatric/sympatric lineages and coupled to the phylogeographic<br />
information obtained. Various post-zygotic isolating mechanisms will be investigated, including<br />
chromosomal incongruence. In this way we also want to illuminate to what extent the frequently used<br />
pre-zygotic clamp connection formation criterion reflects reproductive isolation. Results from some<br />
studies indicate that reinforcement may be an important speciation mechanism in fungi. The importance<br />
of hybridization and reinforcement during fungal speciation will be investigated through the analyses of<br />
hybrid zones and mating experiments between allopatric/sympatric populations. The team behind this<br />
project together shares the expertise and experience needed to carry through all of the proposed<br />
subprojects.<br />
The team<br />
Tor Carlsen (Post Doc), Inger Skrede (Post Doc), Kristian Seierstad (PhD), Håvard Kauserud, Glenn-<br />
Peter Sætre (CEES) + external collaborators.<br />
12<br />
From left: Fruit bodies of Amanita<br />
muscaria (Photo: Arve Græsdal) and<br />
Hypholoma fasciculare (Photo: Per<br />
Marstad)
<strong>MERG</strong><br />
Fungi and climate change<br />
Objectives of the project<br />
• Analyse the effects of climate change on the biology of fungi.<br />
• Analyse the impact of climate change on fungal phenology and fungi’s distribution patterns.<br />
Project summary<br />
It is well-documented that recent climate change has had great effect on biological systems. Climate<br />
change has resulted in changes in the timing of phenological events in many organisms, but relatively<br />
little attention has been paid to how microorganisms, including fungi, respond to climate change. In this<br />
project the aim is to explore which impact climate change has on fungi. In one part of the project we<br />
analyze how the phenology of fungal fruiting bodies has changed in relation to climate change using<br />
complex statistical models. For this purpose we use different types of time series data, including<br />
herbarium records from various European countries. In another part of the project we aim at analysing<br />
how fungi’s distributions will change under future climate scenarios by niche modeling analyses.<br />
The team<br />
Håvard Kauserud, Klaus Høiland, Nils Chr. Stenseth (CEES), Rune Halvorsen (NHM), + external.<br />
13
<strong>MERG</strong><br />
Habitat fragmentation and pathways to extinction in dead-wood<br />
dependent fungi<br />
Objectives of the project<br />
• Study the variables that affect the occurrence of aphyllophorous fungal species (polypores and<br />
corticioids), with a particular focus on how species’ life-history traits are linked with their<br />
vulnerability to the effects of forestry.<br />
• Identify the demographic and genetic processes that disentangle the species that have and have<br />
not responded negatively to forest management and fragmentation.<br />
• Examine the variation in intraspecific genetic diversity and its effects to the viability of<br />
populations.<br />
Project summary<br />
In spite of extensive amount of forest biodiversity research in Fennoscandia, the exact mechanisms<br />
behind species declines are still poorly understood. Identifying the key processes leading to extinctions<br />
is critical for the development of scientifically informed and cost-effective conservation measures, the<br />
prediction of future population trends and the assessment of conservation needs. Our project takes<br />
advantage of the ongoing revolution in molecular biology and sequencing technology, which enables<br />
one to combine conventional fruit-body inventories with direct measurements of the mycelial (drilling<br />
sawdust) and dispersal stages (sampling spores from the air). The project will produce systematic<br />
information on the distribution, abundance and viability of dead-wood dependent fungi as fruit bodies,<br />
mycelia and spores in Sweden and Norway. This information will be used to identify the key<br />
mechanisms behind species declines.<br />
The team<br />
Jenni Nordén (Post Doc), Anders B. Aas, Håvard Kauserud, Karl-Henrik Larsson (NHM) + external<br />
collaborators.<br />
14
<strong>MERG</strong><br />
High throughput sequencing of deep sea metagenomes<br />
Objectives of the project<br />
The objective of this project is to establish high throughput sequencing as a tool for metagenome<br />
investigations of deep sea sediments in the northern regions. Sediments influenced by methane and<br />
hydrocarbons are of special interests.<br />
Our aims within the project are:<br />
• Comparison of microbial diversity at the sea floor and in oil reservoirs at different sites.<br />
• Setting up competence around high throughput sequencing and bioinformatics analysis of<br />
metagenomic data and sharing this competence with collaborators around Norway.<br />
Project Summary<br />
The microbial density in marine sediments is about 10 8 -10 9 microbial cells/cm 3 and is reported to<br />
exceed 10 5 microbial cells/cm 3 even at depths close to 1000 m below the seafloor. 16S rDNA<br />
sequencing has been used to characterize the composition of microbial communities in deep sea gas<br />
hydrate sedimentary systems or active mud volcanoes such as the Håkon Mosby Mud Volcano (HMMV)<br />
in the Barents Sea. These studies confirm that little is known about the microbial consortia in marine<br />
sediments and that only a few of the microbes detected have been cultivated or described before.<br />
Furthermore, it seems clear that the environmental conditions, including the carbon and energy sources<br />
available in the habitat, strongly influences microbial diversity. In this project metagenomics is used to<br />
help us understand which organisms (and their relative proportions) and which genes (i.e.;<br />
biochemistry) are present in different deep sea sediment ecosystems and oil reservoirs. Furthermore,<br />
comparison of samples of different ecosystems makes it possible to identify habitat specific functions,<br />
e.g. metabolic pathways, within the microbial community. In addition it becomes possible to perform<br />
gene hunts, for example for genes (enzymes) involved in degradation of long-chained alkanes. In<br />
principle, any potentially interesting gene can be discovered this way.<br />
The team<br />
Thomas Haverkamp (Post Doc), Othilde Håvelsrud (PhD), Helga Kristiansen (MSc student), Kjetill S.<br />
Jakobsen, Anne Gunn Rike (NGI), Ole Andreas Løchen Økstad (LaMDa), Tom Kristensen,<br />
15
<strong>MERG</strong><br />
Hydrurus foetidus, a large freshwater representative of the<br />
Chromalveolate (SAR?) clade<br />
Objectives of the project<br />
- Clear up the molecular phylogeny of a strain from Finse<br />
- Collect and publish all information on Hydrurus from Norway<br />
- Critically go through all published records of this sp. worlwide<br />
- Based upon environmental information, bring a strain into culture<br />
- Study the evolutionary conditioned plasticity expressed under different culture conditions<br />
From left: Hydrurus foetidus (Photo: Dag Klaveness), Hydrurus foetidus (Photo: Dag Klaveness), Part of Tafel 1 (XV) from<br />
Berthold 1878<br />
Project summary<br />
Hydrurus foetidus (Vill.) Trev. 1843 is a multicellular, arbuscular representative of the golden algae,<br />
appearing seasonally in cold rivers, typically in early spring season during snowmelt. The thallus may<br />
reach considerable dimensions, but under natural conditions a length of 3-10 cm is typical. This alga<br />
has a long history of scientific attention, because its size and morphological plasticity do not fit in<br />
among the typical golden algae – and the fragility of the thallus have resisted any attempt of bringing it<br />
into culture in liquid media, since Rostafinski first tried in 1882. A molecular phylogeny has alredy been<br />
constructed based upon partial 18S and 28S rDNA sequences, without a definitive location among the<br />
chrysophytes – but securely located among the latter. We have solved the basic problems with<br />
culturing, but there remains a lot of thinking to design experimental conditions for the laboratory study<br />
of this obligate psychrophilic rheophile (= low-temperature and highturbulence-dependent organism).<br />
The team<br />
Jon Bråte (PhD), Kamran Shalchian-Tabrizi, Kjetill S. Jakobsen, Nina Værøy (MSc student), Eli-Anne<br />
Lindstrøm, Dag Klaveness<br />
16
<strong>MERG</strong><br />
Microbial ecology of mycorrhizal symbiosis<br />
Objectives of the project<br />
• A main focus will be to analyze which factors that determine and influence on the structure and<br />
composition of the ectomycorrhizal (ECM) fungal community in the Bistorta vivipara root system.<br />
• Using experimental and empirical approaches, we want to analyze the effects of factors like host<br />
genotype (ecotype) and variation in environmental conditions on the ECM community and how the<br />
ECM community changes during a primary successional process.<br />
• Furthermore, we want to analyze the effects of various biotic interactions (like the occurrence of<br />
various bacteria) on the ECM community of B. vivipara.<br />
• Another main task will be to evaluate the temporal and spatial variation in the ECM fungal community<br />
associated with B. vivipara.<br />
A<br />
Project summary<br />
The community ecology of root associated fungi will be studied using the perennial plant Bistorta<br />
vivipara as a ‘model system’. As one of few herbaceous plants, B. vivipara forms ectomycorrhizal (ECM)<br />
relationships with various fungi. The small and condensed root systems makes B. vivipara an ideal<br />
model organism for ECM community studies since the entire fungal assemblage associated with the<br />
roots easily can be analyzed simultaneously using high throughput sequencing technologies. Using B.<br />
vivipara as a model system we will be able to overcome many of the challenges we face when working<br />
with the large root systems of slow-growing cultivated trees. One main focus will be to analyze which<br />
factors that determine and influence on the structure and composition of root-associated fungi of B.<br />
vivipara. We also want to analyze the bacteria associated with the mycorrhizal symbiosis and study the<br />
interplay between the plant host, the fungal symbionts and the associated bacteria. Both observational<br />
field studies and experiments will be conducted. The experiments will involve the establishment of an in<br />
vitro model system, where effects of bacterial and fungal species in the symbiotic relationship will be<br />
tested.<br />
The team<br />
Tor Carlsen (Post Doc), Rakel Blaalid (PhD), Unni Vik (PhD), Fang Yao (MSc-student), Synnøve Botnen<br />
(MSc-student), Rune Heimdal (MSc-student), Håvard Kauserud, Tom Andersen, Klaus Høiland, Trond<br />
Schumacher, Anne-Brit Kolstø (LaMDa), Ole Andreas Løchen Økstad (LaMDa), Anne Brysting (CEES),<br />
Karl I. Ugland (Marine) + external collaborators.<br />
17<br />
B<br />
A. Bistorta vivipara B. The small and<br />
condensed root systems makes B.<br />
vivipara an ideal model organism<br />
for ECM community studies<br />
Photo: Unni Vik<br />
Photo: Marie Davey
<strong>MERG</strong><br />
Origin of animals and plants<br />
Objectives of the project<br />
• Resolve the phylogeny of choanozoa by multi-gene phylogenies<br />
• Mapping the change of genes involved in cell signalling and cell adhesion on the Choanozoa and<br />
early animal phylogeny<br />
• Reveal the earliest occurrence of DAK1 among the plant lineage<br />
• Functional characterization of DAK1 domains in algae and early plant lineages.<br />
• Data-mining and detection of different types of kinases among the Choanozoa.<br />
Project summary<br />
Transition from unicellular to the multicellular eukaryotes have occurred multiple times from different<br />
ancestors, and given rise to plants, animals, fungi, some multicellular amoeba forms, some red and<br />
brown algae as well as few other groups. The molecular basis for the all these transitions and the<br />
formation of the various body plans have likely involved very different components; for instance the<br />
genes involved in embyogenesis of animals seem not to have been central in formation of multicellular<br />
plants.<br />
In this project we investigate the origin and evolution of animals and plants by phylogenomic<br />
analyses. Our approach is to use phylogeny of the opisthokonts (animals, fungi and Choanozoa) and<br />
Viridiplantae (plants and green algae) as a frame for mapping genetic and genomic changes of key<br />
components for cell adhesion and cell signaling. The two projects on animals and plants were initiated<br />
separately and involves different scientists, but a major goal is to compare the evolutionary processes<br />
that lead to multicellularity in these two lineages.<br />
The Team<br />
Marianne Minge, Marit Espelund, Kjetill S. Jakobsen, Ruiz Inaki, Thomas Cavalier-Smith, Odd-Arne<br />
Olsen, Rob Wilson, Kamran Shalchian-Tabrizi<br />
18<br />
From left: Reticulomyxa Filosa Photo:<br />
José Fahrni, Five group of Eukaryotic<br />
organsims<br />
Illustrasjon: Fabian Burki
<strong>MERG</strong><br />
Phylogenomic and single cell whole genome amplification of<br />
Radiolaria<br />
Objectives of the project<br />
• Develop and optimize genome-sequencing methods for unculturable unicellular protists.<br />
• Partially sequence the genome and cDNA sequences from three radiolarian species in order to<br />
provide suitable data for: Investigation of the phylogenetic placement of Radiolaria by using<br />
multigene data (phylogenomics), and, Identification of sequence markers appropriate for<br />
species phylogeny and detection of cryptic species diversity.<br />
• Study the species phylogeny and cryptic diversity of radiolarian lineages by the use of a<br />
phylogenetic species concept and compare the molecular phylogeny with the current<br />
morphology-based systematics of the group.<br />
• Investigate symbionts and parasites associated with the radiolarian cells by using the developed<br />
molecular methods<br />
Callimitra carolotae, Lamprocyclas maritalis, mitrocalpis_araneafera, nephrospyris_knutheieri, Lamprocyclas maritalis. Photo: Kjell Bjørklund<br />
Project summary<br />
A major goal of the project is to develop methods for genomic investigations of unculturable unicellular<br />
eukaryotes, which comprise the vast majority of the species. A method known as single cell whole<br />
genome amplification (SCWGA) can provide enough DNA template for multiple downstream analyses.<br />
The method has not been widely applied on protists and there is therefore a great need for optimization<br />
and development. SCWGA will be coupled with the latest upgrade of the 454-pyrosequencing<br />
technology. Using these techniques we will study a group of unicellular eukaryotes (protists),<br />
Radiolaria, which like most other microorganisms, are notoriously difficult to grow in culture and are<br />
therefore virtually nothing is known about their genomes, ecology and species diversity. Hence this<br />
project will generate knowledge about both advanced molecular methods, applicable for any type of<br />
microorganism, and fundamental knowledge about a very much enigmatic lineage of eukaryotes. The<br />
coupling of SCWGA and 454-pyrosequencing will allow: - Investigation of the gene and genome<br />
organization of at least partial genomes of radiolarians. - Reconstruction of the genome evolution of<br />
members of the eukaryotic supergroup SAR (includes Radiolaria) as several species in SAR have been,<br />
or currently are being, genome sequenced. - Rigorous phylogenetic investigation of Radiolaria using a<br />
multigene approach (phylogenomics). - Identification of proper markers for population genetics and<br />
across-species studies. - Identification and characterization of associated symbionts or parasites.<br />
The team<br />
Jon Bråte (PhD), Anders Krabberød (PhD), Jane Dolven, Tom Kristensen, Randi Ose, Kjell Bjørklund,<br />
Dag Klaveness, Kamran Shalchian-Tabrizi<br />
19
<strong>MERG</strong><br />
Population diversification and horizontal gene transfer processes<br />
in freshwater cyanobacteria: genomic and ecological perspectives<br />
Objectives of the project<br />
• Study whether the subpopulation structure of cyanobacteria in Lake Steinsfjorden and Lake<br />
Kolbotnvannet.<br />
• Compare the cyanobacteria genetic and chemotype diversity in different ecological<br />
environments.<br />
• Investigate the impact of a change in nutrient concentration on the genetic diversity of<br />
Planktothrix strains in Lake Gjersjøen.<br />
• Study to what extent the frequency of HGT is influenced by biotic factors such as Chytrid<br />
(fungal) infection, or abiotic factors (stresses) such as UV- exposure or shaking.<br />
Kolbotnvannet<br />
Photo: Hanne Ballestad<br />
Project summary:<br />
The overall goal of this study is to gain a deeper understanding of cyanobacterial population<br />
diversification processes and how horizontal gene transfer, dispersal and selective forces are<br />
influencing such processes. The long time goal is to achieve an improved understanding of<br />
cyanobacterial population genetics – which in turn should open up for a cyanobacterial species<br />
concept, or a rejection of the species concept. In a study of Planktothrix from Lake Kolbotnvannet we<br />
utilize the NRPS markers and additional markers to study the chemotype/genotype diversity and the<br />
impact of selective pressure on the diversity. Complete genome sequencing by the 454 technology of<br />
several Norwegian and German Planktothrix strains is currently in progress. In a comparative study we<br />
will look into genetic differences between the genomes and search for answers to what significance the<br />
genetic variation has had for the differences in chemotype-diversity between Norwegian and German<br />
freshwaters. We will also do a pan/core genome study to reveal the common set of genes in the genus<br />
Planktothrix and compare it with those of other cyanobacteria. By utilizing field samples from Lake<br />
Gjersjøen from 1964-2008 we will study the historical genotype dynamics and what impact a change in<br />
nutrient availability has had for the genetic diversity of Planktothrix chemotypes. We will also look for an<br />
answer to what impact the genetic diversity has had for the increased biomass of Anabaena. One<br />
hypothesis is that stressors lead to an aggregation and cell lysis and that this may result in a higher<br />
frequency of HGT, and consequently in an increased genetic diversity. If our experimental study<br />
confirms that infection by chytrids results in an increased frequency of HGT, we may look into what<br />
significance higher genotype/chemotype diversity has for cyanobacteria’s resistance against infection<br />
by chytrids.<br />
The team<br />
Hanne Ballestad (PhD), Trine B. Rounge (Post Doc), Ave Tooming-Klunderud (Post Doc), Kjetill S.<br />
Jakobsen, Thomas Rohrlack.<br />
20
<strong>MERG</strong><br />
Population genetics and phylogeography of Serpula lacrymans<br />
Objectives of the project<br />
• Study the phylogeny of Serpula lacrymans and closely related lineages to illuminate the evolutionary<br />
origin of Serpula lacrymans.<br />
• Study the phylogeography of Serpula lacrymans to unravel from where, when, and how it has spread<br />
and colonized the human domain.<br />
• Analyze the population genetics of Serpula lacrymans in order to reveal basic biological traits such<br />
as reproductive mode, degree of clonality and dispersal capacity.<br />
• Study the evolution and spread of mating types within Serpula lacrymans.<br />
Project summary<br />
The dry rot fungus Serpula lacrymans is a severe destroyer of wooden building materials in temperate<br />
regions worldwide. It has an outcrossing (heterothallic) reproductive mode and is able to produce and<br />
spread an enormous amount of basidiospores. It is also capable of local vegetative colonization by<br />
rhizomorphs (i.e. aggregated hyphal structures). Being a widespread aggressive indoor biodeterioration<br />
agent, it has only been found a few times in natural environments. It is still not known when the fungus<br />
established in buildings, but it was probably in connection with the establishment of more permanent<br />
human settlements with wooden constructions, and thus the dry rot fungus probably has a short<br />
evolutionary history in indoor habitats. In this project we want to study basic biological traits of S.<br />
lacrymans, such as dispersal capacity and reproductive mode, true population genetic analyses.<br />
Another aim is to study the evolutionary relationship between S. lacrymans and closely related lineages.<br />
We also want to reveal from where and when S. lacrymans spread out and colonized the human<br />
domain.<br />
The team<br />
Inger Skrede (Post Doc), Sarasvati Jacobsen Bjørnaraa (MSc Student), Håvard Kauserud, + external<br />
collaborators.<br />
21<br />
The dry rot fungus Serpula lacrymans<br />
fruiting in a house.<br />
Photo: Mycoteam AS
<strong>MERG</strong><br />
Saxitoxin biosynthesis and genomics in organisms from two<br />
kingdoms - horizontal gene transfer or parallel evolution?<br />
Objectives of the project<br />
• Investigate the biochemical mechanism and enzymes involved in sxt biosynthesis.<br />
• Identify and characterize saxitoxin genes from several dinoflagellate species. Investigate<br />
evolution, phylogenetic origin, and possible horizontal gene transfer.<br />
Figure 1.<br />
Horizontal Gene Transfer of STX from<br />
cyanobacteria to dinoflagellates?<br />
22<br />
Figure 2.<br />
Alexandrium Photo: Wenche Eikrem<br />
Project summary<br />
Saxitoxin (STX) is a natural neurotoxin produced by certain species of marine cyanobacteria and<br />
dinoflagellates. STX: A secondary metabolite blocks sodium channels, preventing transduction of<br />
neuronal signals. STX distribution is very peculiar; to-date it has only been identified in 2 dinoflagellate<br />
(Dinophyceae) orders (Gymnodiniales and Gonyaulacales) and 2 cyanobacteria orders (Nostocales<br />
and Oscillatoriales). This distribution is intriguing when considering the evolutionary distance between<br />
these orders. The STX gene cluster has been cloned and sequenced for numerous cyanobacteria,<br />
however as yet not for dinoflagellates. Despite this both are presumed to have a similar biosynthetic<br />
pathway. Bacteria living in symbiosis with dinoflagellates do not produce STX so only 2 possible<br />
scenarios explain STX distribution; Firstly, the parallel evolution of traits due to similar environmental<br />
pressures and secondly, the most plausible scenario; Horizontal Gene Transfer (HGT) of STX from<br />
cyanobacteria to dinoflagellates. As STX sequence information is available for cyanobacteria so this<br />
project will focus on dinoflagellates: Toxic dinoflagellate cultures have been obtained and maintained<br />
from 32 Alexandrium strains. DNA has been isolated from these strains and PCR product for 18s (Small<br />
Sub Unit), 5.8s, 28s (Large Sub Unit) and ITS (Internal transcribers) rRNA regions has been amplified<br />
and sequenced. The toxic profile of the strains has been determined with ELISA and Mass<br />
spectrometry. Phylogentic work using rRNA to determine the evolutionary branching pattern within<br />
Alexandrium is in progress.Total RNA has been isolated for 2 Alexandrium strains and has been used to<br />
construct 2 normalized cDNA libraries. The tagged libraries have now been run on 454 titanium<br />
technology. To date the sequencing of a ½ plate has resulted in 13800 contigs for the A. fundyense<br />
library and ~11400 contigs for the A. minutum library. The project is now progressing to a<br />
bioinformatics stage. Firstly, all contigs will have to be annotated in relation to functionality before<br />
checking for presence of STX genes using a multitude of bioinformatic tools (Bioportal).<br />
The Team:<br />
Anke Stüken (Post Doc), Russell Orr (PhD), Ralf Kellman (Bergen), Kamran Shalchian-Tabrizi, Kjetill S.<br />
Jakobsen
<strong>MERG</strong><br />
Regulatory RNA and the origin of animal multicellularity<br />
This is a project in the field of evolutionary developmental (evo-devo) biology. The overall aim is to<br />
greatly improve our understanding of the transition from unicellular eukaryotes to multicellular animals.<br />
This represents a mega-leap in the evolution of eukaryote genome and cell organisation that hence of<br />
fundamental importance in biology and medicine.<br />
Project summary<br />
We will in this project focus on the unicellular relatives of animals termed Choanozoa. On the basis of<br />
current status in the field we aim toward bringing the field of evo-devo a step further by rigorous<br />
examination of the role of non-coding and regulatory RNA in the evolution of animal multicellularity. This<br />
will be achieved by studying selected Choanozoa species and using bioinformatics and highthroughput<br />
sequencing approaches.<br />
Objectives of the project<br />
In this project we will investigate:<br />
• RNAi machinery losses and gains in the genomes of single-celled ancestors of animals<br />
• The miRNA pathway evolution in animals compared to other eukaryotic supergroups<br />
• Whether the miRNA and piRNA pathways have been essential for development of multicellularity<br />
• Regulatory RNAs in single celled Choanoza that are not derived from RNAi precursors<br />
• Evolution and function of the RNAi protein machinery<br />
• Whether genetic processes, such as gene duplications, lineage-specific gene loss or horizontal gene<br />
transfer took part in shaping the regulatory RNA machinery in Choanozoa<br />
The team<br />
Jon Bråte (Post Doc), Ralf Neumann (PhD), Tom Kristensen, Paul Grini, Dag Klaveness, Kamran<br />
Shalchian-Tabrizi, Maja Adamska (SARS, Bergen), Inaki Ruiz (Univ Barcelona, Spain), Yves Van de<br />
Peer (Univ. of Gent, Belgium)<br />
23<br />
Sphaeroeca, a colony of<br />
choanoflagellates (aproximately 230<br />
individuals). Photo: Dhzanette.<br />
Wikimedia Commons
<strong>MERG</strong><br />
X-cell parasites: an emerging threat to marine fish<br />
Objectives of the project<br />
• To determine the ecological and geographical distribution of X-cell lineages, and their<br />
phylogenetic relationships.<br />
• Use FISH microscopy and immuno-staining to elucidate the X-cell lifecycle.<br />
• Use comparative genomics methods to identify how this pathogen infects and interacts with host<br />
and what are the genetic characteristics associated with the process of infection.<br />
• Develop biotechnological tools for detection of X-cells in fish and in the environment for early<br />
warning systems.<br />
Project summary<br />
The term X-cell was first used in 1969 to refer to distinctive cells found in epidermal tumours of flatfish.<br />
Subsequently, cells with a similar appearance have been found in over 25 species of fish. Many of<br />
these are commercially important, and are also farmed, which greatly increases the incidence of<br />
disease and its transmission. X-cell diseases are still mostly unknown, so we currently have a) no way of<br />
knowing how important they really are, b) which so far uncharacterised diseases are caused by X-cells,<br />
and c) no understanding of how to best manage aquaculture systems to minimise X-cell related<br />
disease. Currently the impact of X-cells is likely to be highly underestimated, as many of its effects are<br />
attributed to other, or unknown causes, or not easily recognised.<br />
X-cell disease forms in three main fish tissues, depending on the species infected: large epidermal<br />
tumours in the skin epidermis, fins, head, and inner opercular region, pseudotumours in the<br />
pseudobranchial tissue, and swollen gill filament lesions.<br />
In addition to the commercial interest, X-cell parasites are of much interest because 1) they are disease<br />
causing agents of many groups of fish, yet we know almost nothing about their distribution, lifecycle,<br />
and mode and frequency of infection, and 2) they occupy a key branching position in the tree of life,<br />
being related to many parasites of a wide range of animals, some of which are of significant commercial<br />
importance. They will teach us a lot about the evolution of parasitism in alveolates. Therefore, the<br />
objectives of the project is to close these knowledge gaps, which are of high ecological and<br />
evolutionary importance.<br />
The team<br />
Dag Klaveness, Kamran Shalchian-Tabrizi, Dr Mark Freeman (University of Malaya), Dr David Bass,<br />
(Natural History Museum London), Anders Jørgensen (Norwegian Veterinary Institute).<br />
24<br />
Pseudobranchial pseudotumours in Atlantic<br />
cod Gadus morhua from Iceland. a) Five<br />
cod from the same year-class; two<br />
uninfected fish (top) and three infected fish<br />
(bottom). b) Pseudobranchs have a gill-red<br />
colour in healthy fish and are enlarged and<br />
have a creamy-whitish appearance when<br />
infected (c) (black arrows). Scale bars a =<br />
4 cm, b & c visible. From Freeman et al.<br />
(2011)
<strong>MERG</strong><br />
Annual report 2011<br />
Appendix 2: JIPPI Report<br />
Microbial Evolution Research Group (<strong>MERG</strong>)<br />
Department of Biology<br />
University of <strong>Oslo</strong>
<strong>MERG</strong><br />
What is JIPPI?<br />
The <strong>MERG</strong> JIPPI score system was introduced in during the first<br />
month 2010. It is a web-based five step procedure that should<br />
not take more than 5-10 minutes. It is adopted from National<br />
Veterinary Institute from Ida Skaar and Section of Mycology.<br />
AIM<br />
The aim is to visualise the activities in <strong>MERG</strong> for<br />
internal use as well as for reporting.<br />
It is important for the success of the “utviklingsmiljø”<br />
to credit all activities. It is also used to measure the<br />
deliverable set in the annual plan. It is intended to<br />
inspire all activities not only publications. Each year<br />
the JIPPI money should be used on a social activity<br />
selected by the <strong>MERG</strong> team. A maximum withdrawal<br />
will depend on the budget. In <strong>MERG</strong>s 2010 Budget<br />
30 000 NOKs are granted. This year the money was<br />
used for a dinner at Nodee.<br />
The entries are grouped into 8 main categories:<br />
Publication<br />
1.1 PUBLICATION: Scientific publication<br />
1.2 PUBLICATION: Popular scientific publications<br />
1.3 PUBLICATION: Book publications / Book chapter<br />
1.4 PUBLICATION: Reports<br />
1.5 PUBLICATION: Posters<br />
1.6 PUBLICATION: Congress lecture<br />
1.7 PUBLICATION: Internal presentation/lecture and<br />
popular contribution<br />
Grant applications<br />
2.1 GRANT APPLICATION: Send a large grant<br />
application (NFR/EU/network)<br />
2.2 GRANT APPLICATION: Send a small grant<br />
application (Nansen/legater/UiO)<br />
2.3 GRANT APPLICATION: Funding of large grant<br />
application<br />
2.4 GRANT APPLICATION: Funding of small grant<br />
application<br />
2<br />
Education<br />
3.1 EDUCATION: Graduation of Master<br />
3.2 EDUCATIONS: PhD dissertation<br />
Courses and workshops<br />
4.1 COURSES / WORKSHOPS: Organise<br />
lab/computer lab<br />
4.2 COURSES / WORKSHOPS: Lecture<br />
4.3 COURSES / WORKSHOPS: Course leader<br />
4.4 COURSES/WORKSHOP: Training/Education of<br />
new students or new employees in lab-procedures<br />
4.5 COURSES/WORKSHOP: Further education<br />
(kompetanseheving)<br />
Media<br />
5.1 MEDIA: Radio / Television<br />
Referee<br />
6.1 REFEREE (incl. internal and external)<br />
HSE<br />
7.1 HSE: Internal publications (web) of<br />
method/protocols<br />
7.2 HSE: Implementation of new instrumentation<br />
7.3 HSE: Maintaining good laboratory standards<br />
according to OHS (HMS) handbook and <strong>MERG</strong> rules<br />
7.4 HSE: Remark during internal OHS inspections<br />
(one entry per lab)<br />
7.5 HSE: Closed lab due to breach of OHS<br />
regulations (one entry per lab)<br />
Other<br />
8. OTHERS:<br />
Each year the JIPPI money should be used on a<br />
social activity selected by the <strong>MERG</strong> team.
<strong>MERG</strong><br />
JIPPI numbers 2011<br />
Based on JIPPI reporting 2010 it is possible to compare the<br />
performance and improvement yearly.<br />
Accumulated JIPPI POINTS 2011<br />
The total JIPPI score 2011 was 103 909 this is an<br />
increase of 42% compared to 2010.<br />
Participation<br />
<strong>MERG</strong> consist of 43 members of these 36 have<br />
contributed to one or more entries. The JIPPI score<br />
is announced each month and published on the<br />
web-pages.<br />
Throughout the year participation in the JIPPI<br />
reporting system has been encourage.<br />
Scientific publications: Impact factors<br />
In 2010 78% of the scientific publications have an<br />
impact factor 3<br />
in 2011 versus 2010, 59% versus 56% in 2011. (See<br />
figure page 6.)<br />
JIPPI 2011: 114, 299 points<br />
and 235 entries, compared<br />
to 76, 851 points and 158<br />
entries in 2010.<br />
Categories<br />
The achievement was within the publications with<br />
57% of all entries. 17% of entries are grant<br />
applications
<strong>MERG</strong><br />
Positive trends<br />
Number of scientific publication has increased<br />
from 27 to 31.<br />
There were more and larger grant applications in<br />
2011 than in 2010<br />
In collaboration with Lamda, Glyconor and Tone<br />
Tønjum group a Centre of Excellent application<br />
was submitted. This got excellent marks (6)<br />
Håvard Kauserud applied for a ERC starting grant<br />
The Microlab facilitiy opened in 2011<br />
33 SOP was written in 2011 compered to none in<br />
2010. Showing increase focus on HSE<br />
There seem to be the same involvement in<br />
teaching.<br />
4<br />
Negative trends<br />
• Number of popular scientific presentation<br />
has dropped drastically from 21 to 5.<br />
• Number of poster and congress lecture has<br />
also dropped from 2010 to 2011<br />
• There were no PhD dessitation in 2011<br />
versus 2 in 2010<br />
• There were 3 master graduations in 2011<br />
versus 6 in 2010.
<strong>MERG</strong><br />
Entered activities<br />
1.1. PUBLICATION: Scientific publication<br />
1 Boltovskoy, Demetrio; Kling, Stanley A.; Takahashi, Kozo; Bjørklund, Kjell Rasmus. WORLD ATLAS OF<br />
DISTRIBUTION OF RECENT POLYCYSTINA (RADIOLARIA). Palaeontologia Electronica 2010 Volum 13(3):1-<br />
230<br />
2 Kruglikova, S.B.; Bjørklund, Kjell Rasmus; Dolven, Jane K.; Hammer, Øyvind; Cortese, G. High-rank<br />
polycystine radiolarian taxa as temperature proxies in the Nordic Seas. Stratigraphy 2010 ;Volume 7.(4) s. 265-<br />
281<br />
3 Shalchian-Tabrizi, K, Røberg, K. R, Ree, D. K, Klaveness, D. and Bråte, J. 2011. Marine-freshwater<br />
colonizations of haptophytes inferred from phylogeny of environmental 18S rDNA sequences<br />
4 Klaveness, D. & Lindstrøm,E-A. 2011. Hydrurus foetidus (Chromista, Chrysophyceae): A large freshwater<br />
chromophyte alga in laboratory culture. Phycological Research 59 (2), xx-yy<br />
5 Nilsson RH, Tedersoo L, Lindahl BD, Kjøller R, Carlsen T, Quince C, Abarenkov K, Pennanen T, Stenlid J,<br />
Bruns T, Larsson K-H, Kıljalg U, Kauserud H. 2011. Towards standardization of the description and publication<br />
of next-generation sequencing datasets of fungal communities. New Phytologist, 191, 314-318.<br />
6 Kumar S, Carlsen T, Mevik B-H, Enger P, Blaalid R, Shalchian-Tabrizi K, Kauserud H. 2011. CLOTU: An online<br />
pipeline for processing and clustering of 454 amplicon reads into OTUs followed by taxonomic annotation.<br />
BMC Bioinformatics, accepted.<br />
7 Buntgen U, Kauserud H, Egli S. 2011. Linking climate variability to mushroom productivity and phenology.<br />
Frontiers in Ecology and the Environment, available online<br />
8 Strand DA, Holst-Jensen A, Viljugrein H, Edvardsen B, Klaveness D, Jussila J, Vrålstad T. 2011. Detection and<br />
quantification of the crayfish plague agent in natural waters: direct monitoring approach for aquatic<br />
environments. Diseases of Aquatic Organisms 95: 9-17<br />
9 Orr, R.J.S, Stüken, A, Rundberget, T, Eikrem, W, Jakobsen, K.S, Improved phylogenetic resolution of toxic<br />
and non-toxic Alexandrium strains using a concatenated rDNA approach. Harmful Algae In Press, Corrected<br />
Proof.<br />
10 Krabberød, A. K, Bråte, J, Dolven, J. K, Ose, R. F, Klaveness, D, Kristensen, T, Bjørklund, K. R. and Shalchian-<br />
Tabrizi, K. Radiolaria divided into Polycystina and Spasmaria in combined 18S and 28S rDNA phylogeny.<br />
2001. PLoS ONE<br />
11 Dittami, S.M, Riisberg, I, John, U, Orr, R.J.S, Jakobsen, K.S, Edvardsen, B, Analysis of Expressed Sequence<br />
Tags from the Marine Microalga Pseudochattonella farcimen (Dictyochophyceae). Protist In Press, Corrected<br />
Proof.<br />
12 Skrede I, Engh IB, Binder M, Carlsen T, Kauserud H, Bendiksby M. 2011. Evolutionary history of Serpulaceae<br />
(Basidiomycota): molecular phylogeny, historical biogeography and evidence for a single transition of<br />
nutritional mode. BMC Evolutionary Biology, 11: 230.<br />
13 Kauserud H, Kumar S, Brysting A, Norden J, Carlsen T. 2011. High consistency between replicate 454<br />
pyrosequencing analyses of ectomycorrhizal plant root samples. Mycorrhiza, in press<br />
14 Eastwood et al. The Plant Cell Wall‚ - Decomposing Machinery Underlies the Functional Diversity of Forest<br />
Fungi. Science 333, 762 (2011)<br />
15 Stüken A, Orr RJS, Kellmann R, Murray SA, Neilan BA, et al. (2011) Discovery of nuclear-encoded genes for<br />
the neurotoxin Saxitoxin in dinoflagellates. PLoS ONE 6.<br />
16 Murray SA, Wiese M, Stüken A, Brett S, Kellmann R, et al. (2011) A quantitative molecular assay based on the<br />
gene sxtA to identify saxitoxin-producing harmful algal blooms in marine waters. Appl Environ Microbiol. 77<br />
(19): 7050-7<br />
17 Shalchian-Tabrizi K, Reier-Røberg K, Ree DK, Klaveness D, Bråte J, Marine- Freshwater Colonizations of<br />
Haptophytes Inferred from Phylogeny of Environmental 18S rDNA Sequences, J Eukaryot Microbiol. 2011 Jul-<br />
Aug;58(4):315-8.<br />
18 Anders K. Krabberød, Jon Bråte Jane K. Dolven, Randi F. Ose, Dag Klaveness, Tom Kristensen, Kjell R.<br />
Bjørklund, Kamran Shalchian-Tabrizi, Radiolaria divided into Polycystina and Spasmaria in combined 18S and<br />
28S rDNA phylogeny . PLoS ONE. ISSN 1932-6203. 6(8) . doi: 10.1371/journal.pone.0023526<br />
5
<strong>MERG</strong><br />
19 Guifré Torruella, Romain Derelle, Jordi Paps, B. Franz Lang, Andrew J. Roger, Kamran Shalchian-Tabrizi and<br />
Iñaki Ruiz-Trillo Phylogenetic relationships within the Opisthokonta based on phylogenomic analyses of<br />
conserved single copy protein domains, Mol Biol Evol (2011) first published online July 18, 2011<br />
20 Hans K. Kotlar, Anna Lewin, Jostein Johansen, Mimmi Throne-Holst, Thomas Haverkamp, Sidsel Markussen,<br />
Asgeir Winnberg, Philip Ringrose, Trine Aakvik, Einar Ryeng, Kjetill Jakobsen, Finn Drabløs, Svein Valla High<br />
coverage sequencing of DNA from microorganisms living in an oil reservoir 2.5 kilometres subsurface.<br />
Environmental Microbiology reports<br />
21 Othilde Elise Håvelsrud, Thomas HA Haverkamp, Tom Kristensen, Kjetill S Jakobsen and Anne Gunn Rike A<br />
metagenomic study of methanotrophic microorganisms in Coal Oil Point seep sediments. BMC Microbiology<br />
2011, 11:221<br />
22 Gjessing MC, Davey M, Kvellestad A, Vrålstad T. 2011. Exophiala angulospora causes systemic inflammation<br />
in Atlantic cod Gadus morhua L. Diseases of Aquatic Organisms 96: 209-219<br />
23 Vrålstad T. 2011. ITS, OTUs and beyond - Fungal hyperdiversity calls for supplementary solutions. Molecular<br />
Ecology 20: 2873-2875<br />
24 Vrålstad T, Johnsen SI, Fristad R, Edsmann L, Strand D. 2011. Potent infection reservoir of crayfish plague<br />
now permanently established in Norway. Diseases of Aquatic Organisms 97: 75-83<br />
25 Håkan Berglund, Jenni Hottola, Reijo Penttilä, Juha Siitonen 2011. Linking substrate and habitat requirements<br />
of wood-inhabiting fungi to their regional extinction vulnerability. Ecography 34: 864-875.<br />
26 Eidesen, P.B, Gulden, G, Høiland, K. 2011. Sopptur i busens fotspor. Agarica 31: 35-40.<br />
27 Gabrielsen, Tove M; Minge, Marianne Aastebøl; Espelund, Mari; Tooming-Klunderud, Ave; Patil, Viswanath;<br />
Nederbragt, Alexander Johan; Otis, Christian et al. (2011). Genome Evolution of a Tertiary Dinoflagellate<br />
Plastid. PLoS ONE. ISSN 1932-6203. 6(4), s e19132 . doi: 10.1371/journal.pone.0019132<br />
28 Torruella, Guifré; Derelle, Romain; Paps, Jordi; Lang, B. Franz; Roger, Andrew J.; Shalchian-Tabrizi, Kamran &<br />
Ruiz-Trillo, Iñaki (2011). Phylogenetic relationships within the Opisthokonta based on phylogenomic analyses<br />
of conserved single-copy protein domains. Molecular biology and evolution. ISSN 0737-<br />
4038. 29(2), s 531- 544 . doi: 10.1093/molbev/msr185<br />
29 Klaveness, Dag; Bråte, Jon; Patil, Viswanath; Shalchian-Tabrizi, Kamran; Kluge, Ragnhild; Gislerød, Hans<br />
Ragnar & Jakobsen, Kjetill Sigurd (2011). The 18S and 28S rDNA identity and phylogeny of the common lotic<br />
chrysophyte Hydrurus foetidus. European journal of phycology. ISSN 0967-0262. 46(3), s 282- 291 . doi:<br />
10.1080/15287394.2011.550564<br />
30 Kozubikova, Eva; Vrålstad, Trude; Filipova, Lenka; Petrusek, Adam. 2011. Re-examination of the prevalence of<br />
Aphanomyces astaci in North American crayfish populations in Central Europe by TaqMan MGB real-time<br />
PCR. Diseases of Aquatic Organisms 97: 113-125<br />
1.2. PUBLICATION: Popular scientific publications<br />
1 Livets opprinnelse, en uløst gåte? Populærforedrag for elevene i 7. klasse ved Uranienborg skole, Forskerne<br />
kommer, Uranienborg skoles 125 års jubileum, og UiOs 200 års jubileum. Klaus Høiland<br />
2 Blogginnlegg: Cryptomycota, - en ny stor soppgruppe? Håvard Kauserud, Klaus Høiland<br />
3 Blogginnlegg: Kan vi forvente bedre soppsesonger i Norge med endret klima? Håvard Kauserud<br />
4 Ekte trøffel i Norge? Sopp og Nyttevekster 2: 12-15. Holst-Jensen, A and Vrålstad T. 2011.<br />
5 Menneskegenomet - et tiårsjubileum. argument #3 (2011). Krabberød, A.K.<br />
6 Rørsopper og Skivesopper under mikroskopet av Gro Gulden. Tor Carlsen<br />
7 Livets opprinnelse, en uløst gåte? Populærforedrag for elevene i 7. klasse ved Uranienborg skole, Forskerne<br />
kommer, Uranienborg skoles 125 års jubileum, og UiOs 200 års jubileum, 8. april 2011, Klaus Høiland<br />
8 Livets opprinnelse, en uløst gåte? Åpen dag, <strong>Universitetet</strong> i <strong>Oslo</strong>, 10. mars 2011, Klaus Høiland.<br />
9 Livets opprinnelse, en uløst gåte? Åpen dag, Bjørknes privatskole, 14. april 2011, Klaus Høiland.<br />
1.3 PUBLICATION: Book publications / Book chapter<br />
1.4 PUBLICATION: Reports<br />
1 Annual report 2010 for Bioportal submitted MLS. Kamran Shalchian-Tabrizi<br />
2 Oral presentation of <strong>MERG</strong> at Biofagevaluering meeting with the Research Council of Norway, <strong>Oslo</strong> Plaza, 1<br />
April 2011. Kamran Shalchian-Tabrizi<br />
6
<strong>MERG</strong><br />
1.5 PUBLICATION: Posters<br />
1 Evolutionary history of an endemic alpine plant, Cardamine nipponica (Brassicaceae), at the range periphery<br />
of arctic-alpine sister species, Cardamine bellidifolia. Poster at ESEB2011. Tor Carlsen<br />
2 Radiolaria Divided into Polycystina and Spasmaria in Combined 18S and 28S rDNA Phylogeny. NoMi-11, 2nd<br />
Norwegian Microbiology meeting, Hemsedal 14.-16. sept. Anders K. Krabberød, Jon Bråte, Jane K. Dolven,<br />
Randi F. Ose, Dag Klaveness, Tom Kristensen, Kjell R. Bjørklund and Kamran Shalchian-Tabrizi<br />
3 Fungal - bacterial - plant associations and interactions in the ectomycorrhizal plant Bistorta vivipara. NoMi-11,<br />
2 nd Norwegian Microbiology meeting, Hemsedal 14-16 Sept. Vik, Unni; Carlsen, Tor; Brysting, Anne Krag;<br />
Økstad, Ole Andreas; Kolstø, Anne-Brit; Kauserud, Håvard<br />
4 Changes of genetic diversity within a Planktothrix community, NoMi-11, 2nd Norwegian Microbiology meeting,<br />
Hemsedal 14.-16. sept. Hanne Ballestad, Thomas Rohrlack, Karin Lagesen, Ave Tooming-Kunderud, Kjetill S.<br />
Jakobsen.<br />
1.6 PUBLICATION: Congress lecture<br />
1 MSA 2011 Invited talk, Phylogeography and speciation of boreal wood-inhabiting fungi Tor Carlsen, Kristian<br />
S. Seierstad, Renate M. Fossdal, Inger Skrede, Ingeborg B. Engh, Otto Miettinen, Karl-Henrik Larsson, and<br />
Håvard Kauserud<br />
2 Presentation of Bioinformatics applications at Biomarks EU network meeting in Barcelona 28 March 2011.<br />
Kamran Shalchian-Tabrizi<br />
3 Alge-symposiumet 2011, <strong>Oslo</strong>, 28-29 September. Oral presentation on closing the gaps in Tree of Life.<br />
Kamran Shalchian-Tabrizi<br />
4 Discovery of nuclear-encoded genes for the neurotoxin saxitoxin in dinoflagellates: Lecture at the International<br />
Conference on Modern and Fossil Dinoflagellates, Liverpool, UK, by Anke Stüken on 2nd Sept. 2011: Anke<br />
Stüken, Russell J.S. Orr, Ralf Kellmann, Shauna A. Murray, Brett A. Neilan, Kjetill S. Jakobsen<br />
5 Discovery of nuclear-encoded genes for the neurotoxin saxitoxin in dinoflagellates Lecture at the 2nd<br />
Norwegian Microbiology Meeting, Hemsedal, Norway, by Anke Stüken on Sept. 16th, 2011: Anke Stüken,<br />
Russell J.S. Orr, Ralf Kellmann, Shauna A. Murray, Brett A. Neilan, Kjetill S. Jakobsen<br />
6 Discovery of nuclear-encoded genes for the neurotoxin saxitoxin in dinoflagellates: Lecture at the<br />
Algaesymposiet, <strong>Oslo</strong>, Norway by Anke Stüken und Sept. 28th, 2011. Anke Stüken, Russell J.S. Orr, Ralf<br />
Kellmann, Shauna A. Murray, Brett A. Neilan, Kjetill S. Jakobsen<br />
7 Improved phylogenetic resolution of toxic and non-toxic Alexandrium strains using a concatenated rDNA<br />
approach, Harmful Algae, Volume 10, Issue 6, September 2011, Pages 676-688, ISSN 1568-9883,<br />
10.1016/j.hal.2011.05.003. Russell J.S. Orr, Anke Stüken, Thomas Rundberget, Wenche Eikrem, Kjetill S.<br />
Jakobsen,<br />
8 How does ecological stress influence Planktothrix microdiversity over time, Hanne Ballestad, CEEs conference<br />
2011<br />
9 Uttalt systemisk betennelse hos torsk forårsaket av en hittil ubeskrevet sopp i gruppen Exophiala. Frisk Fiskkonferansen<br />
2011 i regi av Norges Forskningsråd. Radisson Blu Hotel, Tromsø, 19- 20.01.2011. Gjessing,<br />
Mona Cecilie; Davey, Marie; Kvellestad, Agnar; Falk, Knut; Vrålstad, Trude. 2011.<br />
10 Radiolaria divided into Polycystina and Spasmaria in combined 18S and 28S rDNA phylogeny, 2011, VI<br />
European Congress of Protistology, Berlin, Germany, Jon Bråte<br />
1.7 PUBLICATION: Internal presentation/lecture and popular contribution<br />
1 Frokost med Kristine foredrag. Biol. Inst. 8. feb. 2011 Jon Bråte.<br />
2 Talk about 'Fungi and climate change' on Vintersopptreffet 5th of February, Håvard Kauserud<br />
3 Tuesday lunch seminar at <strong>MERG</strong> 16.03.2011 1) Anke Stüken Convergent Evolution or Horizontal Gene<br />
Transfer? 2) Update on the Saxitoxin project, Anke Stüken Russell Orr Kjetill Jakobsen<br />
4 Talk: Habitat fragmentation and pathways to extinction in dead-wood dependent fungi, Jenni Norden<br />
5 Blog posting about the dry rot fungus genome, Håvard Kauserud<br />
6 Blog posting about HTS of fungi, Håvard Kauserud<br />
7 Internal presentation at UWS, Carlsen<br />
8 Ekskursjon, "Lista rundt", veiledet om plantene langs strendene på Lista 6. juli, Klaus Høiland<br />
9 Foredraget "Evolusjonen baklengs" holdt i "Den biologiske fadderuken 2011", Klaus Høiland<br />
10 Tuesday seminar, 23 august, Inger Skrede<br />
7
<strong>MERG</strong><br />
11 Life Science Strategy Meeting for the MN-faculty at Voksenåsen, Tuesday 11 January 2011, Kamran<br />
Shalchian-Tabrizi<br />
12 Presentation of <strong>MERG</strong> at Life Science strategic meeting at MN-faculty - collaboration with University of<br />
Minnesota, 14 June 2011, Kamran Shalchian-Tabrizi<br />
13 Ledet opptur arrangert av biologisk fagutvalg på Bygdøy 3. september 2011, Klaus Høiland<br />
14 Velferdsutvalget ved UiO sin sopptur til Slattum i Nittedal 8. september 2011, Trond Schumacher og Klaus<br />
Høiland<br />
15 Sopptur arrangert av Biologisk institutt til Finnerud i Nordmarka, <strong>Oslo</strong>, 12. september 2011, Trond<br />
Schumacher og Klaus Høiland<br />
16 Ledelse av sopptur arrangert av NFR til Sandbakken i Østmarka, <strong>Oslo</strong>/Enebakk, 14. september 2011, Klaus<br />
Høiland<br />
17 Slørsopptur arrangert av Neslekremla til Vettakollen i Nordmarka, <strong>Oslo</strong>, 17. september 2011, Klaus Høiland<br />
18 Sopp på sanddyner. Foredrag holdt på Høstsopptreffet på Sola, Rogaland, 10. september 2011, Klaus<br />
Høiland<br />
19 Forskningstorget, UiO presentasjon, Biologisk institutt. På stand 14. september 2011, Klaus Høiland<br />
20 Radiolaria revealed as a reservoir for Marine alveolates. VI European Congress of Protistology, Berlin,<br />
Germany, Jon Bråte<br />
21 Frokost hos Kristine 12. april 2011: Biologi og Beatles, Klaus Høiland<br />
22 Frokost hos Kristine 7. september 2011: Er det liv er det sopp, Klaus Høiland<br />
23 Frokost hos Kristine 26. oktober 2011: Sopper på sanddyner på Lista, Klaus Høiland<br />
24 Søndagsforedrag 30. oktober 2011, Zoologisk museum NHM: Norsk furupanel, barndommens<br />
jordbærmarker, valmuene i Penny Lane, biologi og Beatles, Klaus Høiland<br />
25 Høiland, K. 2011. Lykken er ei varm rifle (Biologi og Beatles). Biolog nr. 2 2011: 14-15.<br />
26 Plantene i kulturlandskapet på Lista, foredrag i ”Mannsforeningen” på Lista, 12. oktober 2011, Klaus Høiland.<br />
27 Sopptur “Lista rundt”, til Husebyparken, Farsund, 15. oktober 2011, Klaus Høiland.<br />
28 Høiland, K. 2011. Sopper i sanddyner. Sopp og nyttevekster nr. 3 2011: 18-?<br />
29 Høiland, K, Ryvarden, L. 2011. Sopp og sex – hvor mange kjønn? Sopp og nyttevekster nr. 4 2011: 21-?<br />
30 Departmental talk, Department of Biochemistry and molecular biology, Dalhousie University, October 2011.<br />
Oral presentation on Closing the gaps in Tree of Life. Kamran Shalchian-Tabrizi<br />
31 Oral presentation of BLASTGrabber program, Department of Biochemistry and molecular biology, Dalhousie<br />
University, October 2011, Kamran Shalchian-Tabrizi<br />
32 Mykorrhiza. Populærvitenskapelig foredrag for 2. videregående på <strong>Oslo</strong> Katedralskole 30.09.2011<br />
2.1 GRANT APPLICATION: Send a large grant application (NFR/EU/network)<br />
1 The evolution of ectomycorrhiza - a comparative genomics approach (EvoEcto). NFR FRIMEDBIO, Inger<br />
Skrede, Håvard Kauserud, Tom Kristensen, Kamran Shalchian-Tabrizi<br />
2 Land- Mycorrhizal fungi associated with introduced Picea sitchensis - indigenous or introduced? (Researcher<br />
project - MILJØ2015), Carlsen Kauserud<br />
3 NFR application to the program NORKLIMA entiteled "Climate change effects on arctic fungal communities ? a<br />
metagenomic approach (ArcFun)", Håvard Kauserud, Thomas Haverkamp<br />
4 Centre of Excellence Proposal to Research Council of Norway, Submitted June 2011, Many<br />
5 Research proposal to MLS for a PhD position, Ralf Neumann, Maria Sviland, Kamran Shalchian-Tabrizi<br />
6 Proposal for a core facility named MicroLabs. Proposal submitted MLS 2 September 2011, Kathrine Schou,<br />
Cecilie Mathiesen, Dag Klaveness, Håvard Kauserud, Kamran Shalchian-Tabrizi, 600.000 NOK<br />
7 Research proposal submitted HAVKYST call from Research Council of Norway 31 August 2011, Dag<br />
Klaveness, Rakel Blaalid, Kamran Shalchian-Tabrizi<br />
8 Research proposal submitted Research Council of Norway call FRIMEDBIO, June 2011, Anders Krabberød,<br />
Jon Bråte, Kjell Bjørklund, Tom Kristensen, Kamran Shalchian-Tabrizi<br />
9 Research proposal submitted Research Council of Norway call HAVKYST, Anders Krabberød, Kjell Bjørklund,<br />
Tom Kristensen, Jon Bråte, Kamran Shalchian-Tabrizi<br />
10 ERC starting grant application, Håvard Kauserud,<br />
11 Bråte, J. Regulatory RNA and the origin of multicellularity. FRIMEDBIO NFR, Bråte, J. Shalchian-Tabrizi, K. and<br />
Neumann, R.<br />
12 Likestillingsmidler 2012, Cecilie Mathiesen, Kathrine Schou, Kamran Shalchian-Tabrizi, Håvard Kauserud<br />
585.000 NOK<br />
8
<strong>MERG</strong><br />
13 High throughput cell sorter for microorganisms, AVIT 2012, Cecilie Mathiesen, Kathrine Schou, Kamran<br />
Shalchian-Tabrizi, Håvard Kauserud 4.000.000 NOK<br />
14 Application form for advanced user support (2011) Notur, Kamran Shalchian-Tabrizi,<br />
15 X-CELL - DAG<br />
2.2 GRANT APPLICATION: Send a small grant application<br />
1 Norden, Jenni. Distribution and ecology of wood-inhabiting corticioid fungi. <strong>MERG</strong>. 14.1.2011, Jenni Norden<br />
2 Areal innspill 2012: Samlokaliseringsgruppa, Kamran Shalchian-Tabrizi, Cecilie Mathiesen, Kathrine Schou<br />
3 A grant application to Kapten Carl Stenholms Donationsfond for studying the history of forestry in our study<br />
sites. <strong>MERG</strong>. April 27, 2011, Jenni Norden<br />
4 NOTUR computational resources application for the Bioportal 24 January, Kamran Shalchian-Tabrizi<br />
5 NOTUR advanced user support for integrating Galaxy in the Bioportal, Ralf Neumann, Kamran Shalchian-<br />
Tabrizi<br />
6 Barcoding Marine Life conference at UiO 2012. Proposal submitted Research Council of Norway, Rakel<br />
Blaalid, Anders K. Krabberød, Kathrine Schou, Kamran Shalchian-Tabrizi<br />
7 PROTIS2012 conference at UiO 2012. Proposal submitted Research Council of Norway for financial support,<br />
Kathrine Schou, Ralf Neumann, Jon Bråte, Sen Zhao, Kamran Shalchian-Tabrizi<br />
8 Frode Olsens Minnepris call from MN-faculty, Håvard Kauserud, Kamran Shalchian-Tabrizi<br />
9 MLS – application for research stay abroad – Unni Vik<br />
2.3 GRANT APPLICATION: Funding of large grant application<br />
1 Funding from Norges Forskningsråd for the project: Larsson, K-H, Norden, J, Kauserud, H, Ovaskainen, O et<br />
al. Habitat fragmentation and pathways to extinction in dead-wood dependent fungi Location: NHM, <strong>MERG</strong><br />
25 March 2011. Funding period 1.1.2011-31.12.2013, Jenni Norden, Håvard Kauserud<br />
2 Proposal for a PhD position was granted by MLS, UiO, Ralf Neumann, Maria Sviland, Kamran Shalchian-<br />
Tabrizi<br />
3 Bråte, J. Regulatory RNA and the origin of multicellularity. FRIMEDBIO NFR, Bråte, J, Shalchian-Tabrizi, K. and<br />
Neumann, R.<br />
4 X-CELL - DAG<br />
2.4 GRANT APPLICATION: Funding of small grant application,<br />
1 Skrede, The Leiv Eiriksson mobility programme. Travel grant for three months stay at Harvard University, USA,<br />
Inger Skrede<br />
2 Skrede, Kristine Bonnevie likestillingsstipend. Travel grant for three months stay at Harvard University, USA,<br />
Inger Skrede<br />
3 Skrede, Inger, Fulbright Fundation, Travel grant for stay at Harvard fall 2011, Skrede, Inger<br />
4 A grant from the Kapten Carl Stenholms Donationsfond: Impact of forest history on wood-inhabiting fungi.<br />
<strong>MERG</strong>. June 21, 2011, Jenni Norden<br />
5 MLS – application for research stay abroad – Unni Vik, 14500<br />
6 NOTUR computational resources application for the Bioportal, Kamran Shalchian-Tabrizi<br />
7 NOTUR advanced user support for integrating Galaxy in the Bioportal, Ralf Neumann, Kamran Shalchian-<br />
Tabrizi<br />
3.1 EDUCATION: Graduation of Master<br />
1 Julkunen, Jari. Metsien hvimisen ja pirstoutumisen vaikutukset metsäluonnon monimuotoisuuteen. (Effects of<br />
forest loss and fragmentation on forest biodiversity.) University of Helsinki. February 2011, Julkunen, Jari<br />
(masterstudent), Jenni Norden (medveileder)<br />
2 Christiane Skogli. 2011. Diversitet og artssammensetning av soppendofytter i timotei (Phleum pratense) under<br />
ulike dyrkningsregimer. Masteroppgave, <strong>Universitetet</strong> i <strong>Oslo</strong>, Biologisk Institutt, Microbial Evolution Research<br />
Group, Christiane Skogli (masterstudent), Trude Vrålstad (hovedveileder), Håvard Kauserud (medveileder)<br />
3.2 EDUCATIONS: PhD dissertation<br />
none<br />
9
<strong>MERG</strong><br />
4.1 COURSES / WORKSHOPS: Organise lab/computer lab<br />
1 Organization of "Write-it-right" scientific writing course given by Gadi Rothenburg and Christopher Lowe.<br />
January 27-28th, 2011 @<strong>MERG</strong>, Anke Stüken<br />
2 Bio 1200 botany lab 15.04, Unni Vik<br />
3 Bio 1200 lab botany 29.04, Unni Vik<br />
4 Bio 1200 lab botany 20.05, Unni Vik<br />
5 Alge-symposiumet 2011, <strong>Oslo</strong>, 28-29 September, Kathrine Schou, Kjetill S. Jakobsen, Kamran Shalchian-<br />
Tabrizi<br />
6 Bioportal workshop at Ås, Russell Orr<br />
7 AB201 at UNIS Computer lab - Molecuilar data analyses - Carlsen<br />
8 AB201 - Supervision of semester research project - Bistorta vivipara root associated fungi - Carlsen<br />
4.2 COURSES / WORKSHOPS: Lecture<br />
1 Lecture about microbial diversity and detection on the course 'Kurs i mikroskopering av jordorganismer',<br />
Håvard Kauserud<br />
2 Lecture on the course 'Kurs i mikroskopering av jordorganismer', Dag Klaveness<br />
3 Four lectures given at Bio4260, Håvard Kauserud<br />
4 Parasitic and pathogenic fungi and oomycetes. Bio 4260 double lecture, May 10th 2011, Trude Vrålstad<br />
5 Krabberød, A.K. "Biologiens idehistorie". Lecture at Bio5000, Anders Kristian Krabberød<br />
6 Phylogenetic inferences, Laboratory School at Depatment of Biology Course for Teachers, at UiO 13 April<br />
2011, Kamran Shalchian-Tabrizi<br />
7 Oral presentation of Tree of Life and the Bioportal computational resources at NOTUR conference at UiO, 24<br />
May 2011, Kamran Shalchian-Tabrizi<br />
8 Presentation of <strong>MERG</strong> at workshop organized by Laboratory School at Department of Biology, UiO, 30<br />
September, Kamran Shalchian-Tabrizi<br />
9 14 lectures given at Bio1000, Kamran Shalchian-Tabrizi.<br />
10 Parasittiske og patogene sopp og eggsporesopp. Bio 1200 dobbelforelesning, 22.09.2011, Trude Vrålstad<br />
11 AB201 at UNIS Lectures - Arctic alpine mycology – Tor Carlsen<br />
12 BIO1200 - Lecture -Endophytes – Tor Carlsen<br />
4.3 COURSES / WORKSHOPS: Courseleder<br />
1 Two days workshop on fungal ecology and phenology with 13 participants, Håvard Kauserud<br />
2 One day workshop on 'How to publish and report' environmental NGS data and metadata. 8 participants,<br />
Håvard Kauserud<br />
3 Workshop 'Bioinformatics for metagenomics analyses' 4-8 April, Håvard Kauserud, Kathrine Schou og Thomas<br />
Haverkamp<br />
4 Course leader/organizer for Bio4260, Håvard Kauserud<br />
5 Bio1200 Finse, Unni Vik<br />
6 Bio1200, Finse, Unni Vik<br />
7 Bio 1200 Finse, Unni Vik<br />
8 Field course Bio1200, Vik, Carlsen<br />
9 One week mycology field course in Drøbak (Bio4260/9260), Håvard Kauserud<br />
10 Research project run on the course bio2150, Håvard Kauserud<br />
11 Field course Tomb Bio1200, Hanne Ballestad<br />
4.4 COURSES/WORKSHOP: Training/Education of new students or new employees in lab-procedures<br />
1 Supervising in field and lab - Synnøve, Unni Vik<br />
2 Fieldwork and lab for Fang, Håvard Kauserud, Unni Vik<br />
3 Hjelpelærer på BIO1200, H2011, Synnøve Botnen<br />
4 Fieldwork and training Ella - Iceland – Tor Carlsen<br />
10
<strong>MERG</strong><br />
4.5 COURSES/WORKSHOP: Further education (kompetanseheving)<br />
1 Workshop 'Probabilistic taxonomic classification of NGS reads'. Seili (Finland), May 22-26, Jenni Norden<br />
2 4 months research stay abroad at UWS, Australia, Carlsen<br />
3 3 months research stay abroad at Pringle laboratory, Harvard, US, Inger Skrede<br />
4 Long term conservation of Marine microbial resources, C. Mathiesen<br />
5 Long term conservation of Marine microbial resources, K. Schou<br />
6 Research stay at Lund University, Sweden, to do genome measurements on dinoflagellates and start cooperation<br />
with Rosa I. Figueroa, Anke Stüken<br />
7 2 weeks at the Alfred-Wegener Institute in the group of Uwe John in January/ February 2011 to<br />
start/investigate collaboration possibilities, Anke Stüken<br />
8 Microbial Genomics and metagenomics workshop, JGI, Walnut Creek, Hanne Ballestad<br />
9 Basic course in first aid – Tor Carlsen, Kathrine Schou, Cecilie Mathiesen<br />
5.1 MEDIA: Radio / Television<br />
1 NRK P2, programposten "Ekko", om trøfler og annen sopp. En dag i august. Klaus Høiland, 100<br />
2 NRK P2, programposten "Ekko", om radioaktivitet i sopp, 15. mars 2011, Klaus Høiland.<br />
3 9-timen NRK1, Botanikk og Beatles, 3. november, Klaus Høiland<br />
6.1 REFEREE (inkl. internal and external)<br />
4 External referee of research paper for Molecular Ecology. January 2011, Trude Vrålstad<br />
5 External referee of research paper for Veterinary Microbiology. January 2011, Trude Vrålstad<br />
6 External referee of manuscript for Knowledge and Management of Aquatic Ecosystems (KAME), feb. 2011,<br />
Trude Vrålstad<br />
7 Journal of Plankton Research Scientific paper review, Anke Stüken<br />
8 Silva Fennica, Jenni Norden<br />
9 Review job for Molecular Ecology, Håvard Kauserud<br />
10 Referee for the journal Fungal Ecology, May 2011, Håvard Kauserud<br />
11 External referee for the journal Veterinary Microbiology, April 2011, Trude Vrålstad<br />
12 Referee job for Molecular Ecology, Håvard Kauserud<br />
13 Referee job for Molecular Ecology, Håvard Kauserud<br />
14 Referee for research paper. Molecular Ecology, Inger Skrede<br />
15 for scientific paper. Fungal Biology. June 2011, Inger Skrede<br />
16 Agarica, Unni Vik<br />
17 Review of paper for Taxon, Carlsen<br />
18 Second review, Fungal Biology, Inger Skrede<br />
19 Internal sensor at master course exam, Carlsen<br />
20 External sensor for Bachelor level course at UMB, Carlsen<br />
21 Review for Protist (April 2011), Russell Orr<br />
7.1 OHS: Internal publications (web) of method/protocols<br />
1 Translation of HSE into English, Cecilie Mathiesen, Bodil Pedersen, Translation Company, Cecilie Mathiesen<br />
2 I-SOP-001-Fumehood (1972), C. Mathiesen, K. Schou<br />
3 I-SOP-002.Dorrexdryer, C. Mathiesen, K. Schou<br />
4 I-SOP-003-Fumehood-Energysaver, C. Mathiesen, K. Schou<br />
5 I-SOP-004-Esco-ClassII-BSC, C.Mathiesen, K. Schou<br />
6 S-SOP-001-HCl, C.Mathiesen, K. Schou<br />
7 S-SOP-002-MEA, C. Mathiesen, K. Schou<br />
8 S-SOP-003-LB, C. Mathiesen, K. Schou<br />
9 S-SOP-004-Mycoantib, C.Mathiesen, K. Schou<br />
10 S-SOP-005-PDA, C. Mathiesen, K. Schou<br />
11 P-SOP-001-Ecoonline, C. Mathiesen, K. Schou<br />
12 P-SOP-002-DatabladEcoonline, C.Mathiesen, K. Schou<br />
13 P-SOP-003-knusekuler, C. Mathiesen, K. Schou<br />
11
<strong>MERG</strong><br />
14 P-SOP-004-DNeasy, C. Mathiesen, K. Schou<br />
15 P-SOP-005-TOPOkloning, C. Mathiesen, K. Schou<br />
16 P-SOP-006-DNAisoCTAB, C. Mathiesen, K. Schou<br />
17 P-SOP-007-Isolatoin av røtter, C. Mathiesen, K. Schou<br />
18 P-SOP-008-PCR, C. Mathiesen, K. Schou<br />
19 P-SOP-009-soil-DNA-purif, C. Mathiesen, K. Schou<br />
20 P-SOP-010-Fungistorage, C. Mathiesen, K. Schou<br />
21 I-SOP-005-Termaks, Cecilie Mathiesen, Kathrine Schou<br />
22 I-SOP-008-Autoclave, Cecilie Mathiesen, Kathrine Schou<br />
23 S-SOP-012-Epifloresence microsope Partec, Cecilie Mathiesen, Kathrine Schou<br />
24 S-SOP-005-BG11, Xi Xiang, Kathrine Schou<br />
25 S-SOP-005-5M NaCl, Emelita Nerlie, Kathrine Schou<br />
26 P_SOP_011_454nested_E_v4, Tor Carlsen, Cecilie Mathiesen<br />
27 P_SOP_012_SeqPrep_Norm_E_v4, Tor Carlsen, Cecilie Mathiesen<br />
28 P_SOP_013_Culturing_Cyanobacteria_E_v1, Xi Xiang, Kathrine Schou<br />
29 P_SOP_014_QiaAMP_Blood_E_v1, Cecilie Mathiesen, Kathrine Schou<br />
30 P_SOP_015_Alexandrium_E_v1, Russell Orr, Emelita Nerlie, Kathrine Schou<br />
31 P_SOP_016_ Nucleospin_N_v0 copy, Anders Aas, Cecilie Mathiesen<br />
32 P_SOP_017_ Wizard_N_v0, Anders Aas, Cecilie Mathiesen<br />
8. OTHERS:<br />
1 Intern opponene ved master eksamen for Lars Nersveen (marin biologi), Håvard Kauserud<br />
2 Ordering new Fume cupboards for renovated labs at Department of Biology, in collaboration with Hege Bakke<br />
at CEES, Bodil k Pedersen HMS, TA John Helge Stensrud, MN-innkjøp Arne Hauglund, Kathrine Schou<br />
<strong>MERG</strong>, Cecilie Mathiesen Ledene verneombud, Kathrine Schou, Cecilie Mathiesen<br />
3 Arbeidsmilø 2011, MN seminar for all Department at the Faculty; Cecilie Mathiesen, Trond Schumacher,<br />
Kathrine Schou, Camilla Tømta, Bodil K. Pedersen, Cecilie Mathiesen, Kathrine Schou<br />
4 Evaluation of the Biology courses at UNIS, Svalbard. 24 and 25 March 2011, Håvard Kauserud<br />
5 Evaluation committee work for PhD position, Håvard Kauserud<br />
6 Evaluation commitee work for post doc position, Håvard Kauserud<br />
7 Den gyldne pekestokk? 2010, Tor Carlsen<br />
8 2nd Norwegian Microbiology Meeting (NoMi-11) Organizing committee: Thomas Haverkamp (<strong>MERG</strong> / CEES)<br />
Raimonda Viburiene (Department of Molecular Biosciences) Eric de Muinck (CEES) Espen Brudal (LaMDa /<br />
NSVS) Solveig Fossum-Raunehaug (Institute for Cancer Research / LaMDa) Ingvild Odsbu (Institute for<br />
Cancer Research / LaMDa) http://www.cees.uio.no/calendar/open-events/seminars/nomi-11.html, Thomas<br />
Haverkamp<br />
9 Opening of MicroLabs 2011, Kathrine Schou, Cecilie Mathiesen, Kamran Shalchian-Tabrizi, Håvard Kauserud,<br />
Dag Klaveness, Klaus Høiland, Tor Carlsen, mm<br />
10 New webpages <strong>MERG</strong> 2011, Kathrine Schou, Cecilie Mathiesen, Kamran Shalchian-Tabrizi, Håvard Kauserud,<br />
Jon Bråte<br />
11 Ledet SOP forprosjeket 2011, Cecilie Mathiesen<br />
12 Ledet Teknikkerforum 2011, Kathrine Schou<br />
13 Arrangert Teknikkerforum tur 2011, Kathrine Schou<br />
14 Arbeid med risikovurdering av fremmede storsopper i Norge for Artsdatabanken, Klaus Høiland.<br />
15 Opponent for Martin Kolisko’s PhD dissertation, Dalhousie University, Canada, Kamran Shalchian-Tabrizi<br />
12
<strong>MERG</strong><br />
Annual report 2011<br />
APPENDIX 3: Staff<br />
Microbial Evolution Research Group (<strong>MERG</strong>)<br />
Department of Biology<br />
University of <strong>Oslo</strong>
<strong>MERG</strong><br />
<strong>MERG</strong> staff<br />
“Utviklingsmiljøet” <strong>MERG</strong> has 8 professors, 3 associate<br />
professors, 4 engineers, 6 Post Docs, 17 PhDs and 6 Master<br />
Students representing 8 countries. The gender balance is 44%<br />
females.<br />
Name Supervisor / contact Position<br />
Bente Edvardsen Professor<br />
Dag Klaveness Professor<br />
Kjell Bjørklund Professor<br />
Kjetill S. Jakobsen Professor<br />
Klaus Høiland Professor<br />
Tom Andersen Professor<br />
Tom Kristensen Professor<br />
Trond Schumacher Professor<br />
Håvard Kauserud Associate Professor<br />
Kamran Shalcian-Tabrizi Associate Professor<br />
Trude Vrålstad<br />
Cecilie Mathiesen<br />
Randi Ose<br />
Anders Bjørnsgaard Aas<br />
Associate ProfessorII<br />
Engineer<br />
Engineer<br />
Project engineer<br />
Kathrine Schou Project manager<br />
Emelita Nerlie Research technician<br />
Anke Stüken K. S. Jakobsen Post doc<br />
Inger Skrede T. Schumacher Post doc<br />
Marie Davey H. Kauserud Post doc<br />
Thomas Haverkamp K. S. Jakobsen Post doc<br />
Tor Carlsen H. Kauserud Post doc<br />
Jenni N ordén H. Kauserud Post doc (External)<br />
Ralf Neumann K. Shalchian-Tabrizi PhD<br />
Anders Krabberød K. Shalchian-Tabrizi PhD<br />
David Strand T. Vrålstad PhD<br />
Hanne Ballestad K. S. Jakobsen PhD
<strong>MERG</strong><br />
Jon Bråte K. Shalchian-Tabrizi PhD<br />
Ketil Stoknes K. Høiland PhD<br />
Marit Bjorbekmo K. Shalchian-Tabrizi PhD<br />
Othilde Håvelsrud T. Kristensen PhD<br />
Rakel Blaalid H. Kauserud PhD<br />
Russell Orr K. S. Jakobsen PhD<br />
Sen Zhao D. Klaveness PhD<br />
Sudagar Balasundaram H. Kauserud PhD<br />
Surenda Kumar K. Shalchian-Tabrizi PhD<br />
Øyvind Stensrud T. Schumacher PhD<br />
Unni Vik H. Kauserud PhD<br />
Xi Xiao K. S. Jakobsen PhD<br />
New PhD T. Andersen PhD<br />
Kristian Seierstad H. Kauserud PhD (External)<br />
Teppo Rämä H. Kauserud PhD (External)<br />
Fang Yao H. Kauserud Master student<br />
Helga Kristiansen H. Kauserud Master student<br />
Mariell Negård T. Vrålastad Master student<br />
Nina Værøy D. Klaveness Master student<br />
Rune Heimdal H. Kauserud Master student<br />
Sarasvati Jacobsen Bjørnaraa H. Kauserud Master student<br />
Synnøve Botnen H. Kauserud Master student<br />
3