Magnus Ivarsson

Dr. Magnus Ivarsson

1. Department of Biology, University of Southern Denmark, Campusvej 55, 5230 Odense, Denmark
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Research Focus & Metrics

Academic Career Length

17Years (2010-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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12 September 2014 in Geobiology
Verified
Journal Article
Open access
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SBS. Bengtson
S. Bengtson
MIMagnus Ivarsson
Magnus Ivarsson
AAA. Astolfo
A. Astolfo
VBV. Belivanova
V. Belivanova
CBC. Broman
C. Broman
MSM. Stampanoni
M. Stampanoni
The deep biosphere of the subseafloor crust is believed to contain a significant part of Earth's biomass, but because of the difficulties of directly observing the living organisms, its composition and ecology are poorly known. We report here a consortium of fossilized prokaryotic and eukaryotic micro‐organisms, occupying cavities in deep‐drilled vesicular basalt from the Emperor Seamounts, Pacific Ocean, 67.5 m below seafloor (mbsf). Fungal hyphae provide the framework on which prokaryote‐like organisms are suspended like cobwebs and iron‐oxidizing bacteria form microstromatolites (Frutexites). The spatial inter‐relationships show that the organisms were living at the same time in an integrated fashion, suggesting symbiotic interdependence. The community is contemporaneous with secondary mineralizations of calcite partly filling the cavities. The fungal hyphae frequently extend into the calcite, indicating that they were able to bore into the substrate through mineral dissolution. A symbiotic relationship with chemoautotrophs, as inferred for the observed consortium, may be a pre‐requisite for the eukaryotic colonization of crustal rocks. Fossils thus open a window to the extant as well as the ancient deep biosphere.

12 May 2016 in Frontiers in Microbiology
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Journal Article
Open access
MIMagnus Ivarsson
Magnus Ivarsson
ASAnna Schnürer
Anna Schnürer
SBStefan Bengtson
Stefan Bengtson
Anna NeubeckAnna Neubeck
Anna Neubeck
The recent recognition of fungi in the oceanic igneous crust challenges the understanding of this environment as being exclusively prokaryotic and forces reconsiderations of the ecology of the deep biosphere. Anoxic provinces in the igneous crust are abundant and increase with age and depth of the crust. The presence of anaerobic fungi in deep-sea sediments and on the seafloor introduces a type of organism with attributes of geobiological significance not previously accounted for. Anaerobic fungi are best known from the rumen of herbivores where they produce molecular hydrogen, which in turn stimulates the growth of methanogens. The symbiotic cooperation between anaerobic fungi and methanogens in the rumen enhance the metabolic rate and growth of both. Methanogens and other hydrogen-consuming anaerobic archaea are known from subseafloor basalt; however, the abiotic production of hydrogen is questioned to be sufficient to support such communities. Alternatively, biologically produced hydrogen could serve as a continuous source. Here we propose anaerobic fungi as a source of bioavailable hydrogen in the oceanic crust, and a close interplay between anaerobic fungi and hydrogen-driven prokaryotes.

6 January 2012 in Geology
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Journal Article
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MIMagnus Ivarsson
Magnus Ivarsson
SBStefan Bengtson
Stefan Bengtson
VBVeneta Belivanova
Veneta Belivanova
MSMarco Stampanoni
Marco Stampanoni
FMFederica Marone
Federica Marone
ATAnders Tehler
Anders Tehler
The deep biosphere of subseafloor basalts is thought to consist of mainly prokaryotes (bacteria and archaea). Here we report fossilized filamentous microorganisms from subseafloor basalts interpreted as fossilized fungal hyphae, probably Dikarya, rather than fossilized prokaryotes. The basalts were collected during the Ocean Drilling Program Leg 197 at the Emperor Seamounts, North Pacific Ocean, and the fossilized fungi are observed in carbonate-filled veins and vesicles in samples that represent a depth of ∼150 m below the seafloor. Three-dimensional visualizations using synchrotron-radiation X-ray tomographic microscopy show characteristic fungal morphology of the mycelium-like network, such as frequent branching, anastomosis, and septa. Possible presence of chitin in the hypha walls was detected by staining with Wheat Germ Agglutinin conjugated with Fluorescein Isothiocyanate and examination using fluorescence microscopy. The presence of fungi in subseafloor basalts challenges the present understanding of the deep subseafloor biosphere as being exclusively prokaryotic.

1 January 2018
Verified
Book Chapter
Closed access
MIMagnus Ivarsson
Magnus Ivarsson
SBStefan Bengtson
Stefan Bengtson
HDHenrik Drake
Henrik Drake
Warren R FrancisWarren R Francis
Warren R Francis

21 October 2015 in PLOS ONE
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Journal Article
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MIMagnus Ivarsson
Magnus Ivarsson
SBStefan Bengtson
Stefan Bengtson
HSHenrik Skogby
Henrik Skogby
PLPeter Lazor
Peter Lazor
CBCurt Broman
Curt Broman
FMFederica Marone
Federica Marone
We have after half a century of coordinated scientific drilling gained insight into Earth´s largest microbial habitat, the subseafloor igneous crust, but still lack substantial understanding regarding its abundance, diversity and ecology. Here we describe a fossilized microbial consortium of prokaryotes and fungi at the basalt-zeolite interface of fractured subseafloor basalts from a depth of 240 m below seafloor (mbsf). The microbial consortium and its relationship with the surrounding physical environment are revealed by synchrotron-based X-ray tomographic microscopy (SRXTM), environmental scanning electron microscopy (ESEM), and Raman spectroscopy. The base of the consortium is represented by microstromatolites—remains of bacterial communities that oxidized reduced iron directly from the basalt. The microstromatolites and the surrounding basalt were overlaid by fungal cells and hyphae. The consortium was overgrown by hydrothermally formed zeolites but remained alive and active during this event. After its formation, fungal hyphae bored in the zeolite, producing millimetre-long tunnels through the mineral substrate. The dissolution could either serve to extract metals like Ca, Na and K essential for fungal growth and metabolism, or be a response to environmental stress owing to the mineral overgrowth. Our results show how microbial life may be maintained in a nutrient-poor and extreme environment by close ecological interplay and reveal an effective strategy for nutrient extraction from minerals. The prokaryotic portion of the consortium served as a carbon source for the eukaryotic portion. Such an approach may be a prerequisite for prokaryotic-eukaryotic colonisation of, and persistence in, subseafloor igneous crust.

16 December 2013 in Scientific Reports
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Journal Article
Open access
MIMagnus Ivarsson
Magnus Ivarsson
CBCurt Broman
Curt Broman
ESErik Sturkell
Erik Sturkell
JOJens Ormö
Jens Ormö
SSSandra Siljeström
Sandra Siljeström
SBStefan Bengtson
Stefan Bengtson
Impacts are common geologic features on the terrestrial planets throughout the solar system, and on at least Earth and Mars impacts have induced hydrothermal convection. Impact-generated hydrothermal systems have been suggested to possess the same life supporting capability as hydrothermal systems associated with volcanic activity. However, evidence of fossil microbial colonization in impact-generated hydrothermal systems is scarce in the literature. Here we report of fossilized microorganisms in association with cavity-grown hydrothermal minerals from the 458 Ma Lockne impact structure, Sweden. Based on morphological characteristics the fossilized microorganisms are interpreted as fungi. We further infer the kerogenization of the microfossils, and thus the life span of the fungi, to be contemporaneous with the hydrothermal activity and migration of hydrocarbons in the system. Our results from the Lockne impact structure show that hydrothermal systems associated with impact structures can support colonization by microbial life.