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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

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