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  • 1. Clemmensen, K. E.
    et al.
    Bahr, A.
    Ovaskainen, O.
    Dahlberg, A.
    Ekblad, Alf
    Örebro University, School of Science and Technology.
    Wallander, H.
    Stenlid, J.
    Finlay, R. D.
    Wardle, D. A.
    Lindahl, B. D.
    Roots and associated fungi drive long-term carbon sequestration in boreal forest2013In: Science, ISSN 0036-8075, E-ISSN 1095-9203, Vol. 339, no 6127, p. 1615-1618Article in journal (Refereed)
    Abstract [en]

    Boreal forest soils function as a terrestrial net sink in the global carbon cycle. The prevailing dogma has focused on aboveground plant litter as a principal source of soil organic matter. Using C-14 bomb-carbon modeling, we show that 50 to 70% of stored carbon in a chronosequence of boreal forested islands derives from roots and root-associated microorganisms. Fungal biomarkers indicate impaired degradation and preservation of fungal residues in late successional forests. Furthermore, 454 pyrosequencing of molecular barcodes, in conjunction with stable isotope analyses, highlights root-associated fungi as important regulators of ecosystem carbon dynamics. Our results suggest an alternative mechanism for the accumulation of organic matter in boreal forests during succession in the long-term absence of disturbance.

  • 2. Eudy, James D.
    et al.
    Weston, Michael D.
    Yao, SuFang
    Hoover, Denise M.
    Rehm, Heidi L.
    Ma-Edmonds, Manling
    Yan, Denise
    Ahmad, Iqbal
    Cheng, Jason J.
    Ayuso, Carmen
    Cremers, Cor
    Davenport, Sandra
    Möller, Claes
    Örebro University, School of Health and Medical Sciences.
    Talmadge, Catherine B.
    Beisel, Kirk W.
    Tamayo, Marta
    Morton, Cynthia C.
    Swaroop, Anand
    Kimberling, William J.
    Sumegi, Janos
    Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa1998In: Science, ISSN 0036-8075, E-ISSN 1095-9203, Vol. 280, no 5370, p. 1753-1757Article in journal (Refereed)
    Abstract [en]

    Usher syndrome type IIa (OMIM 276901), an autosomal recessive disorder characterized by moderate to severe sensorineural hearing loss and progressive retinitis pigmentosa, maps to the long arm of human chromosome 1q41 between markers AFM268ZD1 and AFM144XF2. Three biologically important mutations in Usher syndrome type IIa patients were identified in a gene (USH2A) isolated from this critical region. The USH2A gene encodes a protein with a predicted size of 171.5 kilodaltons that has laminin epidermal growth factor and fibronectin type III motifs; these motifs are most commonly observed in proteins comprising components of the basal lamina and extracellular matrixes and in cell adhesion molecules.

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