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  • 1. Abreu, Ilka N.
    et al.
    Johansson, Annika I.
    Sokolowska, Katarzyna
    Niittylä, Totte
    Sundberg, Björn
    Hvidsten, Torgeir R.
    Umeå University, Faculty of Science and Technology, Department of Plant Physiology. Umeå University, Faculty of Science and Technology, Umeå Plant Science Centre (UPSC). Faculty of Chemistry, Biotechnology and Food Science, Norwegian University of Life Sciences, Ås, Norway.
    Street, Nathaniel R.
    Umeå University, Faculty of Science and Technology, Department of Plant Physiology. Umeå University, Faculty of Science and Technology, Umeå Plant Science Centre (UPSC).
    Moritz, Thomas
    A metabolite roadmap of the wood-forming tissue in Populus tremula2020In: New Phytologist, ISSN 0028-646X, E-ISSN 1469-8137, Vol. 228, no 5, p. 1559-1572Article in journal (Refereed)
    Abstract [en]

    Wood, or secondary xylem, is the product of xylogenesis, a developmental process that begins with the proliferation of cambial derivatives and ends with mature xylem fibers and vessels with lignified secondary cell walls. Fully mature xylem has undergone a series of cellular processes, including cell division, cell expansion, secondary wall formation, lignification and programmed cell death. A complex network of interactions between transcriptional regulators and signal transduction pathways controls wood formation. However, the role of metabolites during this developmental process has not been comprehensively characterized. To evaluate the role of metabolites during wood formation, we performed a high spatial resolution metabolomics study of the wood-forming zone of Populus tremula, including laser dissected aspen ray and fiber cells. We show that metabolites show specific patterns within the wood-forming zone, following the differentiation process from cell division to cell death. The data from profiled laser dissected aspen ray and fiber cells suggests that these two cell types host distinctly different metabolic processes. Furthermore, by integrating previously published transcriptomic and proteomic profiles generated from the same trees, we provide an integrative picture of molecular processes, for example, deamination of phenylalanine during lignification is of critical importance for nitrogen metabolism during wood formation.

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  • 2.
    Akhter, Shirin
    et al.
    Department of Plant Biology, Linnean Center for Plant Biology, Uppsala BioCentre, Swedish University of Agricultural Sciences (SLU), Uppsala, Sweden.
    Westrin, Karl Johan
    Science for Life Laboratory, Department of Gene Technology, KTH Royal Institute of Technology, Solna, Sweden.
    Zivi, Nathan
    Department of Plant Biology, Linnean Center for Plant Biology, Uppsala BioCentre, Swedish University of Agricultural Sciences (SLU), Uppsala, Sweden; Skogforsk, Uppsala Science Park, Uppsala, Sweden.
    Nordal, Veronika
    Department of Plant Biology, Linnean Center for Plant Biology, Uppsala BioCentre, Swedish University of Agricultural Sciences (SLU), Uppsala, Sweden.
    Kretzschmar, Warren W.
    Science for Life Laboratory, Department of Gene Technology, KTH Royal Institute of Technology, Solna, Sweden.
    Delhomme, Nicolas
    Department of Forest Genetics and Plant Physiology, Umeå Plant Science Centre, Swedish University of Agricultural Sciences (SLU), Umeå, Sweden.
    Street, Nathaniel R.
    Umeå University, Faculty of Science and Technology, Department of Plant Physiology. Umeå University, Faculty of Science and Technology, Umeå Plant Science Centre (UPSC).
    Nilsson, Ove
    Department of Forest Genetics and Plant Physiology, Umeå Plant Science Centre, Swedish University of Agricultural Sciences (SLU), Umeå, Sweden.
    Emanuelsson, Olof
    Science for Life Laboratory, Department of Gene Technology, KTH Royal Institute of Technology, Solna, Sweden.
    Sundström, Jens F.
    Department of Plant Biology, Linnean Center for Plant Biology, Uppsala BioCentre, Swedish University of Agricultural Sciences (SLU), Uppsala, Sweden.
    Cone-setting in spruce is regulated by conserved elements of the age-dependent flowering pathway2022In: New Phytologist, ISSN 0028-646X, E-ISSN 1469-8137, Vol. 236, no 5, p. 1951-1963Article in journal (Refereed)
    Abstract [en]

    Reproductive phase change is well characterized in angiosperm model species, but less studied in gymnosperms. We utilize the early cone-setting acrocona mutant to study reproductive phase change in the conifer Picea abies (Norway spruce), a gymnosperm. The acrocona mutant frequently initiates cone-like structures, called transition shoots, in positions where wild-type P. abies always produces vegetative shoots.

    We collect acrocona and wild-type samples, and RNA-sequence their messenger RNA (mRNA) and microRNA (miRNA) fractions. We establish gene expression patterns and then use allele-specific transcript assembly to identify mutations in acrocona. We genotype a segregating population of inbred acrocona trees.

    A member of the SQUAMOSA BINDING PROTEIN-LIKE (SPL) gene family, PaSPL1, is active in reproductive meristems, whereas two putative negative regulators of PaSPL1, miRNA156 and the conifer specific miRNA529, are upregulated in vegetative and transition shoot meristems. We identify a mutation in a putative miRNA156/529 binding site of the acrocona PaSPL1 allele and show that the mutation renders the acrocona allele tolerant to these miRNAs. We show co-segregation between the early cone-setting phenotype and trees homozygous for the acrocona mutation.

    In conclusion, we demonstrate evolutionary conservation of the age-dependent flowering pathway and involvement of this pathway in regulating reproductive phase change in the conifer P. abies.

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  • 3.
    Angelcheva, Liudmila
    et al.
    Umeå University, Faculty of Science and Technology, Department of Chemistry.
    Mishra, Yogesh
    Umeå University, Faculty of Science and Technology, Department of Chemistry. Umeå University, Faculty of Science and Technology, Umeå Plant Science Centre (UPSC).
    Antti, Henrik
    Umeå University, Faculty of Science and Technology, Department of Chemistry.
    Kjellsen, Trygve D.
    Department of Biology, Norwegian University of Science and Technology.
    Funk, Christiane
    Umeå University, Faculty of Science and Technology, Department of Chemistry. Umeå University, Faculty of Science and Technology, Umeå Plant Science Centre (UPSC).
    Strimbeck, Richard G.
    Department of Biology, Norwegian University of Science and Technology.
    Schröder, Wolfgang P.
    Umeå University, Faculty of Science and Technology, Department of Chemistry. Umeå University, Faculty of Science and Technology, Umeå Plant Science Centre (UPSC).
    Metabolomic analysis of extreme freezing tolerance in Siberian spruce (Picea obovata)2014In: New Phytologist, ISSN 0028-646X, E-ISSN 1469-8137, Vol. 204, no 3, p. 545-555Article in journal (Refereed)
    Abstract [en]

    Siberian spruce (Picea obovata) is one of several boreal conifer species that can survive at extremely low temperatures (ELTs). When fully acclimated, its tissues can survive immersion in liquid nitrogen. Relatively little is known about the biochemical and biophysical strategies of ELT survival. We profiled needle metabolites using gas chromatography coupled with mass spectrometry (GC-MS) to explore the metabolic changes that occur during cold acclimation caused by natural temperature fluctuations. In total, 223 metabolites accumulated and 52 were depleted in fully acclimated needles compared with pre-acclimation needles. The metabolite profiles were found to develop in four distinct phases, which are referred to as pre-acclimation, early acclimation, late acclimation and fully acclimated. Metabolite changes associated with carbohydrate and lipid metabolism were observed, including changes associated with increased raffinose family oligosaccharide synthesis and accumulation, accumulation of sugar acids and sugar alcohols, desaturation of fatty acids, and accumulation of digalactosylglycerol. We also observed the accumulation of protein and nonprotein amino acids and polyamines that may act as compatible solutes or cryoprotectants. These results provide new insight into the mechanisms of freezing tolerance development at the metabolite level and highlight their importance in rapid acclimation to ELT in P.obovata.

  • 4.
    Atkin, Owen K
    et al.
    Department of Biology, The University of York, PO Box 373, York YO10 5YW, UK.
    Sherlock, David
    Department of Biology, The University of York, PO Box 373, York YO10 5YW, UK.
    Fitter, Alastair H
    Department of Biology, The University of York, PO Box 373, York YO10 5YW, UK.
    Jarvis, Susan
    Department of Biology, The University of York, PO Box 373, York YO10 5YW, UK.
    Hughes, John K
    Department of Biology, The University of York, PO Box 373, York YO10 5YW, UK.
    Campbell, Catherine
    Umeå University, Faculty of Science and Technology, Umeå Plant Science Centre (UPSC).
    Hurry, Vaughan
    Umeå University, Faculty of Science and Technology, Department of Plant Physiology. Umeå University, Faculty of Science and Technology, Umeå Plant Science Centre (UPSC).
    Hodge, Angela
    Department of Biology, The University of York, PO Box 373, York YO10 5YW, UK.
    Temperature dependence of respiration in roots colonized by arbuscular mycorrhizal fungi2009In: New Phytologist, ISSN 0028-646X, E-ISSN 1469-8137, Vol. 182, no 1, p. 188-199Article in journal (Refereed)
    Abstract [en]

    * The arbuscular mycorrhizal (AM) symbiosis is ubiquitous, and the fungus represents a major pathway for carbon movement in the soil-plant system. Here, we investigated the impacts of AM colonization of Plantago lanceolata and temperature on the regulation of root respiration (R). * Warm-grown AM plants exhibited higher rates of R than did nonAM plants, irrespective of root mass. AM plants exhibited higher maximal rates of R (R(max)-R measured in the presence of an uncoupler and exogenous substrate) and greater proportional use of R(max) as a result of increased energy demand and/or substrate supply. The higher R values exhibited by AM plants were not associated with higher maximal rates of cytochrome c oxidase (COX) or protein abundance of either the COX or the alternative oxidase. * Arbuscular mycorrhizal colonization had no effect on the short-term temperature dependence (Q(10)) of R. Cold-acclimated nonAM plants exhibited higher rates of R than their warm-grown nonAM counterparts. By contrast, chilling had a negligible effect on R of AM-plants. Thus, AM plants exhibited less cold acclimation than their nonAM counterparts. * Overall, these results highlight the way in which AM colonization alters the underlying components of respiratory metabolism and the response of root R to sustained changes in growth temperature.

  • 5.
    Augusti, Angela
    et al.
    Umeå University, Faculty of Science and Technology, Department of Plant Physiology. Umeå University, Faculty of Science and Technology, Umeå Plant Science Centre (UPSC).
    Betson, Tatiana R
    Umeå University, Faculty of Medicine, Department of Medical Biochemistry and Biophysics.
    Schleucher, Jürgen
    Umeå University, Faculty of Medicine, Department of Medical Biochemistry and Biophysics.
    Hydrogen exchange during cellulose synthesis distinguishes climatic and biochemical isotope fractionations in tree rings.2006In: New Phytologist, ISSN 0028-646X, E-ISSN 1469-8137, Vol. 172, no 3, p. 490-499Article in journal (Refereed)
    Abstract [en]

    • The abundance of the hydrogen isotope deuterium (D) in tree rings is an attractive record of climate; however, use of this record has proved difficult so far, presumably because climatic and physiological influences on D abundance are difficult to distinguish.

    • Using D labelling, we created a D gradient in trees. Leaf soluble sugars of relatively low D abundance entered cellulose synthesis in stems containing strongly D-labelled water. We used nuclear magnetic resonance (NMR) spectroscopy to quantify D in the C-H groups of leaf glucose and of tree-ring cellulose.

    • Ratios of D abundances of individual C-H groups of leaf glucose depended only weakly on leaf D labelling, indicating that the D abundance pattern was determined by physiological influences. The D abundance pattern of tree-ring cellulose revealed C-H groups that exchanged strongly (C(2)-H) or weakly (C(6)-H2) with water during cellulose synthesis.

    • We propose that strongly exchanging C-H groups of tree-ring cellulose adopt a climate signal stemming from the D abundance of source water. C-H groups that exchange weakly retain their D abundance established in leaf glucose, which reflects physiological influences. Combining both types of groups may allow simultaneous reconstruction of climate and physiology from tree rings.

  • 6. Augusti, Angela
    et al.
    Schleucher, Jürgen
    Umeå University, Faculty of Medicine, Department of Medical Biochemistry and Biophysics.
    The ins and outs of stable isotopes in plants.2007In: New Phytologist, ISSN 0028-646X, E-ISSN 1469-8137, Vol. 174, no 3, p. 473-475Article in journal (Refereed)
  • 7. Bai, Bing
    et al.
    Novák, Ondrej
    Ljung, Karin
    Hanson, Johannes
    Umeå University, Faculty of Science and Technology, Umeå Plant Science Centre (UPSC). Umeå University, Faculty of Science and Technology, Department of Plant Physiology. Molecular Plant Physiology, Institute of Environmental Biology, Utrecht University, 3584 CH Utrecht, the Netherlands.
    Bentsink, Leonie
    Combined transcriptome and translatome analyses reveal a role for tryptophan-dependent auxin biosynthesis in the control of DOG1-dependent seed dormancy2018In: New Phytologist, ISSN 0028-646X, E-ISSN 1469-8137, Vol. 217, no 3, p. 1077-1085Article in journal (Refereed)
    Abstract [en]

    The importance of translational regulation during Arabidopsis seed germination has been shown previously. Here the role of transcriptional and translational regulation during seed imbibition of the very dormant DELAY OF GERMINATION 1 (DOG1) near-isogenic line was investigated. Polysome profiling was performed on dormant and after-ripened seeds imbibed for 6 and 24 h in water and in the transcription inhibitor cordycepin. Transcriptome and translatome changes were investigated. Ribosomal profiles of after-ripened seeds imbibed in cordycepin mimic those of dormant seeds. The polysome occupancy of mRNA species is not affected by germination inhibition, either as a result of seed dormancy or as a result of cordycepin treatment, indicating the importance of the regulation of transcript abundance. The expression of auxin metabolism genes is discriminative during the imbibition of after-ripened and dormant seeds, which is confirmed by altered concentrations of indole-3-acetic acid conjugates and precursors.

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  • 8.
    Bai, Bing
    et al.
    Department of Molecular Plant Physiology, Utrecht University, 3584 CH Utrecht, the Netherlands; Wageningen Seed Laboratory, Laboratory of Plant Physiology, Wageningen University, 6708 PB Wageningen, the Netherlands.
    Peviani, Alessia
    van der Horst, Sjors
    Gamm, Magdalena
    Snel, Berend
    Bentsink, Leónie
    Hanson, Johannes
    Umeå University, Faculty of Science and Technology, Department of Plant Physiology. Department of Molecular Plant Physiology, Utrecht University, 3584 CH Utrecht, the Netherlands.
    Extensive translational regulation during seed germination revealed by polysomal profiling2017In: New Phytologist, ISSN 0028-646X, E-ISSN 1469-8137, Vol. 214, no 1, p. 233-244Article in journal (Refereed)
    Abstract [en]

    This work investigates the extent of translational regulation during seed germination. The polysome occupancy of each gene is determined by genome-wide profiling of total mRNA and polysome-associated mRNA. This reveals extensive translational regulation during Arabidopsis thaliana seed germination. The polysome occupancy of thousands of individual mRNAs changes to a large extent during the germination process. Intriguingly, these changes are restricted to two temporal phases (shifts) during germination, seed hydration and germination. Sequence features, such as upstream open reading frame number, transcript length, mRNA stability, secondary structures, and the presence and location of specific motifs correlated with this translational regulation. These features differed significantly between the two shifts, indicating that independent mechanisms regulate translation during seed germination. This study reveals substantial translational dynamics during seed germination and identifies development-dependent sequence features and cis elements that correlate with the translation control, uncovering a novel and important layer of gene regulation during seed germination.

  • 9.
    Bittencourt, Paulo Roberto de Lima
    et al.
    College of Life and Environmental Sciences, University of Exeter, Exeter, United Kingdom.
    Bartholomew, David
    Umeå University, Faculty of Science and Technology, Department of Ecology and Environmental Sciences. College of Life and Environmental Sciences, University of Exeter, Exeter, United Kingdom.
    Banin, Lindsay F.
    UK Centre for Ecology & Hydrology, Penicuik, Midlothian, United Kingdom.
    Bin Suis, Mohamed Aminur Faiz
    Sabah Forestry Department, Forest Research Centre, PO Box 1407, Sabah, Sandakan, Malaysia.
    Nilus, Reuben
    Sabah Forestry Department, Forest Research Centre, PO Box 1407, Sabah, Sandakan, Malaysia.
    Burslem, David F. R. P.
    School of Biological Sciences, University of Aberdeen, Aberdeen, United Kingdom.
    Rowland, Lucy
    College of Life and Environmental Sciences, University of Exeter, Exeter, United Kingdom.
    Divergence of hydraulic traits among tropical forest trees across topographic and vertical environment gradients in Borneo2022In: New Phytologist, ISSN 0028-646X, E-ISSN 1469-8137, Vol. 235, no 6, p. 2183-2198Article in journal (Refereed)
    Abstract [en]

    Fine-scale topographic–edaphic gradients are common in tropical forests and drive species spatial turnover and marked changes in forest structure and function. We evaluate how hydraulic traits of tropical tree species relate to vertical and horizontal spatial niche specialization along such a gradient. Along a topographic–edaphic gradient with uniform climate in Borneo, we measured six key hydraulic traits in 156 individuals of differing heights in 13 species of Dipterocarpaceae. We investigated how hydraulic traits relate to habitat, tree height and their interaction on this gradient. Embolism resistance increased in trees on sandy soils but did not vary with tree height. By contrast, water transport capacity increased on sandier soils and with increasing tree height. Habitat and height only interact for hydraulic efficiency, with slope for height changing from positive to negative from the clay-rich to the sandier soil. Habitat type influenced trait–trait relationships for all traits except wood density. Our data reveal that variation in the hydraulic traits of dipterocarps is driven by a combination of topographic–edaphic conditions, tree height and taxonomic identity. Our work indicates that hydraulic traits play a significant role in shaping forest structure across topographic–edaphic and vertical gradients and may contribute to niche specialization among dipterocarp species.

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  • 10.
    Blume-Werry, Gesche
    et al.
    Umeå University, Faculty of Science and Technology, Department of Ecology and Environmental Sciences. Experimental Plant Ecology, Institute of Botany and Landscape Ecology, Greifswald University, Greifswald, Germany.
    Dorrepaal, Ellen
    Umeå University, Faculty of Science and Technology, Department of Ecology and Environmental Sciences.
    Keuper, Frida
    BioEcoAgro Joint Research Unit, INRAE, Barenton-Bugny, France.
    Kummu, Matti
    Water and Development Research Group, Aalto University, Aalto, Finland.
    Wild, Birgit
    Department of Environmental Science, Stockholm University, Stockholm, Sweden; Bolin Centre for Climate Research, Stockholm University, Stockholm, Sweden.
    Weedon, James T.
    Amsterdam Institute for Life and Environment (A-LIFE), Systems Ecology Section, Vrije Universiteit Amsterdam, Amsterdam, Netherlands.
    Arctic rooting depth distribution influences modelled carbon emissions but cannot be inferred from aboveground vegetation type2023In: New Phytologist, ISSN 0028-646X, E-ISSN 1469-8137, Vol. 240, no 2, p. 502-514Article in journal (Refereed)
    Abstract [en]

    The distribution of roots throughout the soil drives depth-dependent plant–soil interactions and ecosystem processes, particularly in arctic tundra where plant biomass, is predominantly belowground. Vegetation is usually classified from aboveground, but it is unclear whether such classifications are suitable to estimate belowground attributes and their consequences, such as rooting depth distribution and its influence on carbon cycling. We performed a meta-analysis of 55 published arctic rooting depth profiles, testing for differences both between distributions based on aboveground vegetation types (Graminoid, Wetland, Erect-shrub, and Prostrate-shrub tundra) and between ‘Root Profile Types’ for which we defined three representative and contrasting clusters. We further analyzed potential impacts of these different rooting depth distributions on rhizosphere priming-induced carbon losses from tundra soils. Rooting depth distribution hardly differed between aboveground vegetation types but varied between Root Profile Types. Accordingly, modelled priming-induced carbon emissions were similar between aboveground vegetation types when they were applied to the entire tundra, but ranged from 7.2 to 17.6 Pg C cumulative emissions until 2100 between individual Root Profile Types. Variations in rooting depth distribution are important for the circumpolar tundra carbon-climate feedback but can currently not be inferred adequately from aboveground vegetation type classifications.

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  • 11.
    Blume-Werry, Gesche
    et al.
    Umeå University, Faculty of Science and Technology, Department of Ecology and Environmental Sciences. Experimental Plant Ecology, Institute of Botany and Landscape Ecology, Greifswald University, Germany.
    Milbau, Ann
    Umeå University, Faculty of Science and Technology, Department of Ecology and Environmental Sciences. Research Institute for Nature and Forest INBO, Brussels, Belgium.
    Teuber, Laurenz M.
    Umeå University, Faculty of Science and Technology, Department of Ecology and Environmental Sciences. Experimental Plant Ecology, Institute of Botany and Landscape Ecology, Greifswald, Germany.
    Johansson, Margareta
    Dorrepaal, Ellen
    Umeå University, Faculty of Science and Technology, Department of Ecology and Environmental Sciences.
    Dwelling in the deep – strongly increased root growth and rooting depth enhance plant interactions with thawing permafrost soil2019In: New Phytologist, ISSN 0028-646X, E-ISSN 1469-8137, Vol. 223, no 3, p. 1328-1339Article in journal (Refereed)
    Abstract [en]

    Climate‐warming‐induced permafrost thaw exposes large amounts of carbon and nitrogen in soil at considerable depths, below the seasonally thawing active layer. The extent to which plant roots can reach and interact with these hitherto detached, deep carbon and nitrogen stores remains unknown.

    We aimed to quantify how permafrost thaw affects root dynamics across soil depths and plant functional types compared with above‐ground abundance, and potential consequences for plant–soil interactions.

    A decade of experimental permafrost thaw strongly increased total root length and growth in the active layer, and deep roots invaded the newly thawed permafrost underneath. Root litter input to soil across all depths was 10 times greater with permafrost thaw. Root growth timing was unaffected by experimental permafrost thaw but peaked later in deeper soil, reflecting the seasonally receding thaw front. Deep‐rooting species could sequester 15N added at the base of the ambient active layer in October, which was after root growth had ceased.

    Deep soil organic matter that has long been locked up in permafrost is thus no longer detached from plant processes upon thaw. Whether via nutrient uptake, carbon storage, or rhizosphere priming, plant root interactions with thawing permafrost soils may feed back on our climate both positively and negatively.

  • 12.
    Blume-Werry, Gesche
    et al.
    Umeå University, Faculty of Science and Technology, Department of Ecology and Environmental Sciences.
    Semenchuk, Philipp
    Department of Arctic Biology, UNIS – The University Centre in Svalbard, Longyearbyen, Norway.
    Ljung, Karin
    Department of Forest Genetics and Plant Physiology, Umeå Plant Science Centre, Swedish University of Agricultural Sciences, Umeå, Sweden.
    Milbau, Ann
    Umeå University, Faculty of Science and Technology, Department of Ecology and Environmental Sciences.
    Novak, Ondrej
    Department of Forest Genetics and Plant Physiology, Umeå Plant Science Centre, Swedish University of Agricultural Sciences, Umeå, Sweden; Laboratory of Growth Regulators, Faculty of Science, Palacký University & Institute of Experimental Botany of the Czech Academy of Sciences, Olomouc, Czech Republic.
    Olofsson, Johan
    Umeå University, Faculty of Science and Technology, Department of Ecology and Environmental Sciences.
    Brunoni, Federica
    Department of Forest Genetics and Plant Physiology, Umeå Plant Science Centre, Swedish University of Agricultural Sciences, Umeå, Sweden; Laboratory of Growth Regulators, Faculty of Science, Palacký University & Institute of Experimental Botany of the Czech Academy of Sciences, Olomouc, Czech Republic.
    In situ seasonal patterns of root auxin concentrations and meristem length in an arctic sedge2024In: New Phytologist, ISSN 0028-646X, E-ISSN 1469-8137, Vol. 242, no 3, p. 988-999Article in journal (Refereed)
    Abstract [en]
    • Seasonal dynamics of root growth play an important role in large-scale ecosystem processes; they are largely governed by growth regulatory compounds and influenced by environmental conditions. Yet, our knowledge about physiological drivers of root growth is mostly limited to laboratory-based studies on model plant species.
    • We sampled root tips of Eriophorum vaginatum and analyzed their auxin concentrations and meristem lengths biweekly over a growing season in situ in a subarctic peatland, both in surface soil and at the permafrost thawfront.
    • Auxin concentrations were almost five times higher in surface than in thawfront soils and increased over the season, especially at the thawfront. Surprisingly, meristem length showed an opposite pattern and was almost double in thawfront compared with surface soils. Meristem length increased from peak to late season in the surface soils but decreased at the thawfront.
    • Our study of in situ seasonal dynamics in root physiological parameters illustrates the potential for physiological methods to be applied in ecological studies and emphasizes the importance of in situ measurements. The strong effect of root location and the unexpected opposite patterns of meristem length and auxin concentrations likely show that auxin actively governs root growth to ensure a high potential for nutrient uptake at the thawfront.
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  • 13.
    Blume-Werry, Gesche
    et al.
    Umeå University, Faculty of Science and Technology, Department of Ecology and Environmental Sciences.
    Wilson, Scott D.
    Umeå University, Faculty of Science and Technology, Department of Ecology and Environmental Sciences. Department of Biology, University of Regina, Regina, Saskatchewan S4S 0A2 Canada.
    Kreyling, Juergen
    Milbau, Ann
    Umeå University, Faculty of Science and Technology, Department of Ecology and Environmental Sciences. Research Institute for Nature and Forest INBO, Kliniekstraat 25, 1070 Brussels, Belgium.
    The hidden season: growing season is 50% longer below than above ground along an arctic elevation gradient2016In: New Phytologist, ISSN 0028-646X, E-ISSN 1469-8137, Vol. 209, no 3, p. 978-986Article in journal (Refereed)
    Abstract [en]

    There is compelling evidence from experiments and observations that climate warming prolongs the growing season in arctic regions. Until now, the start, peak, and end of the growing season, which are used to model influences of vegetation on biogeochemical cycles, were commonly quantified using above-ground phenological data. Yet, over 80% of the plant biomass in arctic regions can be below ground, and the timing of root growth affects biogeochemical processes by influencing plant water and nutrient uptake, soil carbon input and microbial activity. We measured timing of above- and below-ground production in three plant communities along an arctic elevation gradient over two growing seasons. Below-ground production peaked later in the season and was more temporally uniform than above-ground production. Most importantly, the growing season continued c. 50% longer below than above ground. Our results strongly suggest that traditional above-ground estimates of phenology in arctic regions, including remotely sensed information, are not as complete a representation of whole-plant production intensity or duration, as studies that include root phenology. We therefore argue for explicit consideration of root phenology in studies of carbon and nutrient cycling, in terrestrial biosphere models, and scenarios of how arctic ecosystems will respond to climate warming.

  • 14.
    Bollhöner, Benjamin
    et al.
    Umeå University, Faculty of Science and Technology, Department of Plant Physiology. Umeå University, Faculty of Science and Technology, Umeå Plant Science Centre (UPSC).
    Jokipii-Lukkari, Soile
    Umeå University, Faculty of Science and Technology, Department of Plant Physiology. Umeå University, Faculty of Science and Technology, Umeå Plant Science Centre (UPSC).
    Bygdell, Joakim
    Umeå University, Faculty of Science and Technology, Department of Chemistry.
    Stael, Simon
    Adriasola, Mathilda
    Muñiz, Luis
    Umeå University, Faculty of Science and Technology, Department of Plant Physiology. Umeå University, Faculty of Science and Technology, Umeå Plant Science Centre (UPSC).
    Van Breusegem, Frank
    Ezcurra, Inés
    Wingsle, Gunnar
    Tuominen, Hannele
    Umeå University, Faculty of Science and Technology, Department of Plant Physiology. Umeå University, Faculty of Science and Technology, Umeå Plant Science Centre (UPSC).
    The function of two type II metacaspases in woody tissues of Populus trees2018In: New Phytologist, ISSN 0028-646X, E-ISSN 1469-8137, Vol. 217, no 4, p. 1551-1565Article in journal (Refereed)
    Abstract [en]

    Metacaspases (MCs) are cysteine proteases that are implicated in programmed cell death of plants. AtMC9 (Arabidopsis thaliana Metacaspase9) is a member of the Arabidopsis MC family that controls the rapid autolysis of the xylem vessel elements, but its downstream targets in xylem remain uncharacterized. PttMC13 and PttMC14 were identified as AtMC9 homologs in hybrid aspen (Populustremulaxtremuloides). A proteomic analysis was conducted in xylem tissues of transgenic hybrid aspen trees which carried either an overexpression or an RNA interference construct for PttMC13 and PttMC14. The proteomic analysis revealed modulation of levels of both previously known targets of metacaspases, such as Tudor staphylococcal nuclease, heat shock proteins and 14-3-3 proteins, as well as novel proteins, such as homologs of the PUTATIVE ASPARTIC PROTEASE3 (PASPA3) and the cysteine protease RD21 by PttMC13 and PttMC14. We identified here the pathways and processes that are modulated by PttMC13 and PttMC14 in xylem tissues. In particular, the results indicate involvement of PttMC13 and/or PttMC14 in downstream proteolytic processes and cell death of xylem elements. This work provides a valuable reference dataset on xylem-specific metacaspase functions for future functional and biochemical analyses.

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  • 15.
    Bollhöner, Benjamin
    et al.
    Umeå University, Faculty of Science and Technology, Department of Plant Physiology. Umeå University, Faculty of Science and Technology, Umeå Plant Science Centre (UPSC).
    Zhang, Bo
    Umeå University, Faculty of Science and Technology, Department of Plant Physiology. Umeå University, Faculty of Science and Technology, Umeå Plant Science Centre (UPSC).
    Stael, Simon
    Denancé, Nicolas
    Overmyer, Kirk
    Goffner, Deborah
    Van Breusegem, Frank
    Tuominen, Hannele
    Umeå University, Faculty of Science and Technology, Department of Plant Physiology. Umeå University, Faculty of Science and Technology, Umeå Plant Science Centre (UPSC).
    Post mortem function of AtMC9 in xylem vessel elements2013In: New Phytologist, ISSN 0028-646X, E-ISSN 1469-8137, Vol. 200, no 2, p. 498-510Article in journal (Refereed)
    Abstract [en]

    Cell death of xylem elements is manifested by rupture of the tonoplast and subsequent autolysis of the cellular contents. Metacaspases have been implicated in various forms of plant cell death but regulation and execution of xylem cell death by metacaspases remains unknown. Analysis of the type II metacaspase gene family in Arabidopsis thaliana supported the function of METACASPASE 9 (AtMC9) in xylem cell death. Progression of xylem cell death was analysed in protoxylem vessel elements of 3-d-old atmc9 mutant roots using reporter gene analysis and electron microscopy. Protoxylem cell death was normally initiated in atmc9 mutant lines, but detailed electron microscopic analyses revealed a role for AtMC9 in clearance of the cell contents post mortem, that is after tonoplast rupture. Subcellular localization of fluorescent AtMC9 reporter fusions supported a post mortem role for AtMC9. Further, probe-based activity profiling suggested a function of AtMC9 on activities of papain-like cysteine proteases. Our data demonstrate that the function of AtMC9 in xylem cell death is to degrade vessel cell contents after vacuolar rupture. We further provide evidence on a proteolytic cascade in post mortem autolysis of xylem vessel elements and suggest that AtMC9 is part of this cascade.

  • 16.
    Brunoni, Federica
    et al.
    Umeå University, Faculty of Science and Technology, Department of Plant Physiology. Umeå University, Faculty of Science and Technology, Umeå Plant Science Centre (UPSC). Umeå Plant Science Centre, Department of Forest Genetics and PlantPhysiology, Swedish University of Agricultural Sciences (SLU), 90183, Umeå, Sweden.
    Collani, Silvio
    Umeå University, Faculty of Science and Technology, Umeå Plant Science Centre (UPSC). Umeå University, Faculty of Science and Technology, Department of Plant Physiology.
    Casanova-Saez, Ruben
    Simura, Jan
    Karady, Michal
    Schmid, Markus
    Umeå University, Faculty of Science and Technology, Umeå Plant Science Centre (UPSC). Umeå University, Faculty of Science and Technology, Department of Plant Physiology.
    Ljung, Karin
    Bellini, C
    Umeå University, Faculty of Science and Technology, Umeå Plant Science Centre (UPSC). Umeå University, Faculty of Science and Technology, Department of Plant Physiology. Institut Jean-Pierre Bourgin, INRAE, AgroParisTech, Université Paris-Saclay, 78000, Versailles, France.
    Conifers exhibit a characteristic inactivation of auxin to maintain tissue homeostasis2020In: New Phytologist, ISSN 0028-646X, E-ISSN 1469-8137, Vol. 226, no 6, p. 1753-1765Article in journal (Refereed)
    Abstract [en]

    Dynamic regulation of the concentration of the natural auxin (IAA) is essential to coordinate most of the physiological and developmental processes and responses to environmental changes. Oxidation of IAA is a major pathway to control auxin concentrations in angiosperms and, along with IAA conjugation, to respond to perturbation of IAA homeostasis. However, these regulatory mechanisms remain poorly investigated in conifers. To reduce this knowledge gap, we investigated the different contributions of the IAA inactivation pathways in conifers. MS-based quantification of IAA metabolites under steady-state conditions and after perturbation was investigated to evaluate IAA homeostasis in conifers. Putative Picea abies GH3 genes (PaGH3) were identified based on a comprehensive phylogenetic analysis including angiosperms and basal land plants. Auxin-inducible PaGH3 genes were identified by expression analysis and their IAA-conjugating activity was explored. Compared to Arabidopsis, oxidative and conjugative pathways differentially contribute to reduce IAA concentrations in conifers. We demonstrated that the oxidation pathway plays a marginal role in controlling IAA homeostasis in spruce. By contrast, an excess of IAA rapidly activates GH3-mediated irreversible conjugation pathways. Taken together, these data indicate that a diversification of IAA inactivation mechanisms evolved specifically in conifers.

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  • 17.
    Brunoni, Federica
    et al.
    Laboratory of Growth Regulators, Institute of Experimental Botany of the Czech Academy of Sciences, Faculty of Science of Palacký University, Olomouc, Czech Republic.
    Pěnčík, Aleš
    Laboratory of Growth Regulators, Institute of Experimental Botany of the Czech Academy of Sciences, Faculty of Science of Palacký University, Olomouc, Czech Republic.
    Žukauskaitė, Asta
    Department of Chemical Biology, Faculty of Science, Palacký University, Olomouc, Czech Republic.
    Ament, Anita
    Laboratory of Growth Regulators, Institute of Experimental Botany of the Czech Academy of Sciences, Faculty of Science of Palacký University, Olomouc, Czech Republic.
    Kopečná, Martina
    Department of Experimental Biology, Faculty of Science, Palacký University, Olomouc, Czech Republic.
    Collani, Silvio
    Umeå University, Faculty of Science and Technology, Department of Plant Physiology. Umeå University, Faculty of Science and Technology, Umeå Plant Science Centre (UPSC).
    Kopečný, David
    Department of Experimental Biology, Faculty of Science, Palacký University, Olomouc, Czech Republic.
    Novák, Ondřej
    Laboratory of Growth Regulators, Institute of Experimental Botany of the Czech Academy of Sciences, Faculty of Science of Palacký University, Olomouc, Czech Republic.
    Amino acid conjugation of oxIAA is a secondary metabolic regulation involved in auxin homeostasis2023In: New Phytologist, ISSN 0028-646X, E-ISSN 1469-8137, Vol. 238, no 6, p. 2264-2270Article in journal (Refereed)
  • 18.
    Bruxaux, Jade
    et al.
    Umeå University, Faculty of Science and Technology, Department of Ecology and Environmental Sciences. Umeå University, Faculty of Science and Technology, Umeå Plant Science Centre (UPSC).
    Zhao, Wei
    Umeå University, Faculty of Science and Technology, Department of Ecology and Environmental Sciences. Umeå University, Faculty of Science and Technology, Umeå Plant Science Centre (UPSC).
    Hall, David
    Umeå University, Faculty of Science and Technology, Department of Ecology and Environmental Sciences. Umeå University, Faculty of Science and Technology, Umeå Plant Science Centre (UPSC). Forestry Research Institute of Sweden (Skogforsk), Sävar, Sweden.
    Curtu, Alexandru Lucian
    Department of Silviculture, Transilvania University of Braşov, Braşov, Romania.
    Androsiuk, Piotr
    Department of Plant Physiology, Genetics and Biotechnology, Faculty of Biology and Biotechnology, University of Warmia and Mazury in Olsztyn, Olsztyn, Poland.
    Drouzas, Andreas D.
    Laboratory of Systematic Botany and Phytogeography, School of Biology, Aristotle University of Thessaloniki, Thessaloniki, Greece.
    Gailing, Oliver
    Department of Forest Genetics and Forest Tree Breeding, University of Göttingen, Göttingen, Germany.
    Konrad, Heino
    Department of Forest Biodiversity and Nature Conservation, Unit of Ecological Genetics, Austrian Research Centre for Forests (BFW), Vienna, Austria.
    Sullivan, Alexis R.
    Umeå University, Faculty of Science and Technology, Department of Ecology and Environmental Sciences. Umeå University, Faculty of Science and Technology, Umeå Plant Science Centre (UPSC).
    Semerikov, Vladimir
    Institute of Plant and Animal Ecology, Ural Division of Russian Academy of Sciences, Ekaterinburg, Russian Federation.
    Wang, Xiao-Ru
    Umeå University, Faculty of Science and Technology, Department of Ecology and Environmental Sciences.
    Scots pine – panmixia and the elusive signal of genetic adaptation2024In: New Phytologist, ISSN 0028-646X, E-ISSN 1469-8137, Vol. 243, no 3, p. 1231-1246Article in journal (Refereed)
    Abstract [en]

    Scots pine is the foundation species of diverse forested ecosystems across Eurasia and displays remarkable ecological breadth, occurring in environments ranging from temperate rainforests to arid tundra margins. Such expansive distributions can be favored by various demographic and adaptive processes and the interactions between them.

    To understand the impact of neutral and selective forces on genetic structure in Scots pine, we conducted range-wide population genetic analyses on 2321 trees from 202 populations using genotyping-by-sequencing, reconstructed the recent demography of the species and examined signals of genetic adaptation.

    We found a high and uniform genetic diversity across the entire range (global FST 0.048), no increased genetic load in expanding populations and minor impact of the last glacial maximum on historical population sizes. Genetic-environmental associations identified only a handful of single-nucleotide polymorphisms significantly linked to environmental gradients.

    The results suggest that extensive gene flow is predominantly responsible for the observed genetic patterns in Scots pine. The apparent missing signal of genetic adaptation is likely attributed to the intricate genetic architecture controlling adaptation to multi-dimensional environments. The panmixia metapopulation of Scots pine offers a good study system for further exploration into how genetic adaptation and plasticity evolve under gene flow and changing environment.

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  • 19.
    Campbell, Catherine D
    et al.
    Umeå University, Faculty of Science and Technology, Department of Plant Physiology. Umeå University, Faculty of Science and Technology, Umeå Plant Science Centre (UPSC). Department of Biology (Area 2), University of York, York, United Kingdom.
    Atkinson, Lindsey
    Zaragoza-Castells, Joana
    Lundmark, Maria
    Umeå University, Faculty of Science and Technology, Department of Plant Physiology. Umeå University, Faculty of Science and Technology, Umeå Plant Science Centre (UPSC).
    Atkin, Owen
    Hurry, Vaughan
    Umeå University, Faculty of Science and Technology, Department of Plant Physiology. Umeå University, Faculty of Science and Technology, Umeå Plant Science Centre (UPSC).
    Acclimation of photosynthesis and respiration is asynchronous in response to changes in temperature regardless of plant functional group2007In: New Phytologist, ISSN 0028-646X, E-ISSN 1469-8137, Vol. 176, no 2, p. 375-389Article in journal (Refereed)
    Abstract [en]

    • Gas exchange, fluorescence, western blot and chemical composition analyses were combined to assess if three functional groups (forbs, grasses and evergreen trees/shrubs) differed in acclimation of leaf respiration (R) and photosynthesis (A) to a range of growth temperatures (7, 14, 21 and 28°C).

    • When measured at a common temperature, acclimation was greater for R than for A and differed between leaves experiencing a 10-d change in growth temperature (PE) and leaves newly developed at each temperature (ND). As a result, the R : A ratio was temperature dependent, increasing in cold-acclimated plants. The balance was largely restored in ND leaves. Acclimation responses were similar among functional groups.

    • Across the functional groups, cold acclimation was associated with increases in nonstructural carbohydrates and nitrogen. Cold acclimation of R was associated with an increase in abundance of alternative and/or cytochrome oxidases in a species-dependent manner. Cold acclimation of A was consistent with an initial decrease and subsequent recovery of thylakoid membrane proteins and increased abundance of proteins involved in the Calvin cycle.

    • Overall, the results point to striking similarities in the extent and the biochemical underpinning of acclimation of R and A among contrasting functional groups differing in overall rates of metabolism, chemical composition and leaf structure.

  • 20.
    Castaño, Carles
    et al.
    Department of Forest Mycology and Plant Pathology, Swedish University of Agricultural Sciences, Uppsala, Sweden.
    Hallin, Sara
    Department of Forest Mycology and Plant Pathology, Swedish University of Agricultural Sciences, Uppsala, Sweden.
    Egelkraut, Dagmar
    Department of Biological Sciences, University of Bergen, Bergen, Norway.
    Lindahl, Björn D.
    Department of Soil and Environment, Swedish University of Agricultural Sciences, Uppsala, Sweden.
    Olofsson, Johan
    Umeå University, Faculty of Science and Technology, Department of Ecology and Environmental Sciences.
    Clemmensen, Karina Engelbrecht
    Department of Forest Mycology and Plant Pathology, Swedish University of Agricultural Sciences, Uppsala, Sweden.
    Contrasting plant–soil–microbial feedbacks stabilize vegetation types and uncouple topsoil C and N stocks across a subarctic–alpine landscape2023In: New Phytologist, ISSN 0028-646X, E-ISSN 1469-8137, Vol. 238, no 6, p. 2621-2633Article in journal (Refereed)
    Abstract [en]

    Global vegetation regimes vary in belowground carbon (C) and nitrogen (N) dynamics. However, disentangling large-scale climatic controls from the effects of intrinsic plant–soil–microbial feedbacks on belowground processes is challenging. In local gradients with similar pedo-climatic conditions, effects of plant–microbial feedbacks may be isolated from large-scale drivers. Across a subarctic–alpine mosaic of historic grazing fields and surrounding heath and birch forest, we evaluated whether vegetation-specific plant–microbial feedbacks involved contrasting N cycling characteristics and C and N stocks in the organic topsoil. We sequenced soil fungi, quantified functional genes within the inorganic N cycle, and measured 15N natural abundance. In grassland soils, large N stocks and low C : N ratios associated with fungal saprotrophs, archaeal ammonia oxidizers, and bacteria capable of respiratory ammonification, indicating maintained inorganic N cycling a century after abandoned reindeer grazing. Toward forest and heath, increasing abundance of mycorrhizal fungi co-occurred with transition to organic N cycling. However, ectomycorrhizal fungal decomposers correlated with small soil N and C stocks in forest, while root-associated ascomycetes associated with small N but large C stocks in heath, uncoupling C and N storage across vegetation types. We propose that contrasting, positive plant–microbial feedbacks stabilize vegetation trajectories, resulting in diverging soil C : N ratios at the landscape scale.

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  • 21. Catford, Jane A.
    et al.
    Jansson, Roland
    Umeå University, Faculty of Science and Technology, Department of Ecology and Environmental Sciences.
    Drowned, buried and carried away: effects of plant traits on the distribution of native and alien species in riparian ecosystems2014In: New Phytologist, ISSN 0028-646X, E-ISSN 1469-8137, Vol. 204, no 1, p. 19-36Article, review/survey (Refereed)
    Abstract [en]

    Riparian vegetation is exposed to stress from inundation and hydraulic disturbance, and is often rich in native and alien plant species. We describe 35 traits that enable plants to cope with riparian conditions. These include traits for tolerating or avoiding anoxia and enabling underwater photosynthesis, traits that confer resistance and resilience to hydraulic disturbance, and attributes that facilitate dispersal, such as floating propagules. This diversity of life-history strategies illustrates that there are many ways of sustaining life in riparian zones, which helps to explain high riparian biodiversity. Using community assembly theory, we examine how adaptations to inundation, disturbance and dispersal shape plant community composition along key environmental gradients, and how human actions have modified communities. Dispersal-related processes seem to explain many patterns, highlighting the influence of regional processes on local species assemblages. Using alien plant invasions like an (uncontrolled) experiment in community assembly, we use an Australian and a global dataset to examine possible causes of high degrees of riparian invasion. We found that high proportions of alien species in the regional species pools have invaded riparian zones, despite not being riparian specialists, and that riparian invaders disperse in more ways, including by water and humans, than species invading other ecosystems.

  • 22. Chahtane, Hicham
    et al.
    Zhang, Bo
    Norberg, Mikael
    LeMasson, Marie
    Thevenon, Emmanuel
    Bakó, László
    Umeå University, Faculty of Science and Technology, Department of Plant Physiology. Umeå University, Faculty of Science and Technology, Umeå Plant Science Centre (UPSC).
    Benlloch, Reyes
    Holmlund, Mattias
    Parcy, Francois
    Nilsson, Ove
    Vachon, Gilles
    LEAFY activity is post-transcriptionally regulated by BLADE ON PETIOLE2 and CULLIN3 in Arabidopsis2018In: New Phytologist, ISSN 0028-646X, E-ISSN 1469-8137, Vol. 220, no 2, p. 579-592Article in journal (Refereed)
    Abstract [en]

    The Arabidopsis LEAFY (LFY) transcription factor is a key regulator of floral meristem emergence and identity. LFY interacts genetically and physically with UNUSUAL FLORAL ORGANS, a substrate adaptor of CULLIN1-RING ubiquitin ligase complexes (CRL1). The functionally redundant genes BLADE ON PETIOLE1 (BOP1) and -2 (BOP2) are potential candidates to regulate LFY activity and have recently been shown to be substrate adaptors of CULLIN3 (CUL3)-RING ubiquitin ligases (CRL3). We tested the hypothesis that LFY activity is controlled by BOPs and CUL3s in plants and that LFY is a substrate for ubiquitination by BOP-containing CRL3 complexes. When constitutively expressed, LFY activity is fully dependent on BOP2 as well as on CUL3A and B to regulate target genes such as APETALA1 and to induce ectopic flower formation. We also show that LFY and BOP2 proteins interact physically and that LFY-dependent ubiquitinated species are produced invitro in a reconstituted cell-free CRL3 system in the presence of LFY, BOP2 and CUL3. This new post-translational regulation of LFY activity by CRL3 complexes makes it a unique transcription factor subjected to a positive dual regulation by both CRL1 and CRL3 complexes and suggests a novel mechanism for promoting flower development.

  • 23.
    Chowdhury, Jamil
    et al.
    Umeå University, Faculty of Science and Technology, Department of Plant Physiology. Umeå University, Faculty of Science and Technology, Umeå Plant Science Centre (UPSC). Department of Forest Genetics and Plant Physiology, Umeå Plant Science Center, Swedish University of Agricultural Sciences, Umeå, Sweden.
    Kemppainen, Minna
    Laboratory of Molecular Mycology, Department of Science and Technology, Institute of Basic and Applied Microbiology, National University of Quilmes (UNQ), and National Scientific and Technical Research Council (CONICET), Bernal, Argentina.
    Delhomme, Nicolas
    Department of Forest Genetics and Plant Physiology, Umeå Plant Science Center, Swedish University of Agricultural Sciences, Umeå, Sweden.
    Shutava, Iryna
    Umeå University, Faculty of Science and Technology, Department of Plant Physiology. Umeå University, Faculty of Science and Technology, Umeå Plant Science Centre (UPSC).
    Zhou, Jingjing
    Umeå University, Faculty of Science and Technology, Department of Plant Physiology. Umeå University, Faculty of Science and Technology, Umeå Plant Science Centre (UPSC). Department of Forest Genetics and Plant Physiology, Umeå Plant Science Center, Swedish University of Agricultural Sciences, Umeå, Sweden.
    Takahashi, Junko
    Department of Forest Genetics and Plant Physiology, Umeå Plant Science Center, Swedish University of Agricultural Sciences, Umeå, Sweden.
    Pardo, Alejandro G.
    Laboratory of Molecular Mycology, Department of Science and Technology, Institute of Basic and Applied Microbiology, National University of Quilmes (UNQ), and National Scientific and Technical Research Council (CONICET), Bernal, Argentina.
    Lundberg-Felten, Judith
    Department of Forest Genetics and Plant Physiology, Umeå Plant Science Center, Swedish University of Agricultural Sciences, Umeå, Sweden.
    Laccaria bicolor pectin methylesterases are involved in ectomycorrhiza development with Populus tremula × Populus tremuloides2022In: New Phytologist, ISSN 0028-646X, E-ISSN 1469-8137, Vol. 236, no 2, p. 639-655Article in journal (Refereed)
    Abstract [en]
    • The development of ectomycorrhizal (ECM) symbioses between soil fungi and tree roots requires modification of root cell walls. The pectin-mediated adhesion between adjacent root cells loosens to accommodate fungal hyphae in the Hartig net, facilitating nutrient exchange between partners. We investigated the role of fungal pectin modifying enzymes in Laccaria bicolor for ECM formation with Populus tremula × Populus tremuloides.
    • We combine transcriptomics of cell-wall-related enzymes in both partners during ECM formation, immunolocalisation of pectin (Homogalacturonan, HG) epitopes in different methylesterification states, pectin methylesterase (PME) activity assays and functional analyses of transgenic L. bicolor to uncover pectin modification mechanisms and the requirement of fungal pectin methylesterases (LbPMEs) for ECM formation.
    • Immunolocalisation identified remodelling of pectin towards de-esterified HG during ECM formation, which was accompanied by increased LbPME1 expression and PME activity. Overexpression or RNAi of the ECM-induced LbPME1 in transgenic L. bicolor lines led to reduced ECM formation. Hartig Nets formed with LbPME1 RNAi lines were shallower, whereas those formed with LbPME1 overexpressors were deeper.
    • This suggests that LbPME1 plays a role in ECM formation potentially through HG de-esterification, which initiates loosening of adjacent root cells to facilitate Hartig net formation.
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  • 24. Cormier, Marc-André
    et al.
    Werner, Roland A.
    Sauer, Peter E.
    Gröcke, Darren R.
    Leuenberger, Markus C.
    Wieloch, Thomas
    Umeå University, Faculty of Medicine, Department of Medical Biochemistry and Biophysics.
    Schleucher, Jürgen
    Umeå University, Faculty of Medicine, Department of Medical Biochemistry and Biophysics.
    Kahmen, Ansgar
    2H-fractionations during the biosynthesis of carbohydrates and lipids imprint a metabolic signal on the δ2H values of plant organic compounds2018In: New Phytologist, ISSN 0028-646X, E-ISSN 1469-8137, Vol. 218, no 2, p. 479-491Article in journal (Refereed)
    Abstract [en]

    Hydrogen (H) isotope ratio (δ2H) analyses of plant organic compounds have been applied to assess ecohydrological processes in the environment despite a large part of the δ2H variability observed in plant compounds not being fully elucidated.

    We present a conceptual biochemical model based on empirical H isotope data that we generated in two complementary experiments that clarifies a large part of the unexplained variability in the δ2H values of plant organic compounds.

    The experiments demonstrate that information recorded in the δ2H values of plant organic compounds goes beyond hydrological signals and can also contain important information on the carbon and energy metabolism of plants. Our model explains where 2H‐fractionations occur in the biosynthesis of plant organic compounds and how these 2H‐fractionations are tightly coupled to a plant's carbon and energy metabolism. Our model also provides a mechanistic basis to introduce H isotopes in plant organic compounds as a new metabolic proxy for the carbon and energy metabolism of plants and ecosystems.

    Such a new metabolic proxy has the potential to be applied in a broad range of disciplines, including plant and ecosystem physiology, biogeochemistry and palaeoecology.

  • 25.
    De La Torre, Amanda R.
    et al.
    Umeå University, Faculty of Science and Technology, Department of Ecology and Environmental Sciences.
    Wang, Tongli
    Jaquish, Barry
    Aitken, Sally N.
    Adaptation and exogenous selection in a Picea glauca x Picea engelmannii hybrid zone: implications for forest management under climate change2014In: New Phytologist, ISSN 0028-646X, E-ISSN 1469-8137, Vol. 201, no 2, p. 687-699Article in journal (Refereed)
    Abstract [en]

    The nature of selection responsible for the maintenance of the economically and ecologically important Picea glaucaxPicea engelmannii hybrid zone was investigated. Genomic, phenotypic and climatic data were used to test assumptions of hybrid zone maintenance and to model future scenarios under climate change. Genome-wide estimates of admixture based on a panel of 86 candidate gene single nucleotide polymorphisms were combined with long-term quantitative data on growth and survival (over 20yr), as well as one-time assessments of bud burst and bud set phenology, and cold hardiness traits. A total of 15498 individuals were phenotyped for growth and survival. Our results suggest that the P.glaucaxP.engelmannii hybrid zone is maintained by local adaptation to growing season length and snowpack (exogenous selection). Hybrids appeared to be fitter than pure species in intermediate environments, which fits expectations of the bounded hybrid superiority model of hybrid zone maintenance. Adaptive introgression from parental species has probably contributed to increased hybrid fitness in intermediate habitats. While P.engelmannii ancestry is higher than P.glauca ancestry in hybrid populations, on average, selective breeding in managed hybrid populations is shifting genomic composition towards P.glauca, potentially pre-adapting managed populations to warmer climates.

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  • 26.
    Derba-Maceluch, Marta
    et al.
    Department of Forest Genetics and Plant Physiology, Umeå Plant Science Centre, Swedish University of Agricultural Sciences, Umeå, Sweden.
    Mitra, Madhusree
    Department of Forest Genetics and Plant Physiology, Umeå Plant Science Centre, Swedish University of Agricultural Sciences, Umeå, Sweden.
    Hedenström, Mattias
    Umeå University, Faculty of Science and Technology, Department of Chemistry.
    Liu, Xiaokun
    Department of Forest Genetics and Plant Physiology, Umeå Plant Science Centre, Swedish University of Agricultural Sciences, Umeå, Sweden.
    Gandla, Madhavi Latha
    Umeå University, Faculty of Science and Technology, Department of Chemistry.
    Barbut, Félix R.
    Department of Forest Genetics and Plant Physiology, Umeå Plant Science Centre, Swedish University of Agricultural Sciences, Umeå, Sweden.
    Abreu, Ilka N.
    Department of Forest Genetics and Plant Physiology, Umeå Plant Science Centre, Swedish University of Agricultural Sciences, Umeå, Sweden.
    Donev, Evgeniy N.
    Department of Forest Genetics and Plant Physiology, Umeå Plant Science Centre, Swedish University of Agricultural Sciences, Umeå, Sweden.
    Urbancsok, János
    Department of Forest Genetics and Plant Physiology, Umeå Plant Science Centre, Swedish University of Agricultural Sciences, Umeå, Sweden.
    Moritz, Thomas
    Department of Forest Genetics and Plant Physiology, Umeå Plant Science Centre, Swedish University of Agricultural Sciences, Umeå, Sweden.
    Jönsson, Leif J.
    Umeå University, Faculty of Science and Technology, Department of Chemistry.
    Tsang, Adrian
    Centre for Structural and Functional Genomics, Concordia University, QC, Montreal, Canada.
    Powlowski, Justin
    Centre for Structural and Functional Genomics, Concordia University, QC, Montreal, Canada.
    Master, Emma R.
    Department of Chemical Engineering and Applied Chemistry, University of Toronto, 200 College Street, ON, Toronto, Canada.
    Mellerowicz, Ewa J.
    Department of Forest Genetics and Plant Physiology, Umeå Plant Science Centre, Swedish University of Agricultural Sciences, Umeå, Sweden.
    Xylan glucuronic acid side chains fix suberin-like aliphatic compounds to wood cell walls2023In: New Phytologist, ISSN 0028-646X, E-ISSN 1469-8137, Vol. 238, no 1, p. 297-312Article in journal (Refereed)
    Abstract [en]

    Wood is the most important repository of assimilated carbon in the biosphere, in the form of large polymers (cellulose, hemicelluloses including glucuronoxylan, and lignin) that interactively form a composite, together with soluble extractives including phenolic and aliphatic compounds. Molecular interactions among these compounds are not fully understood.

    We have targeted the expression of a fungal α-glucuronidase to the wood cell wall of aspen (Populus tremula L. × tremuloides Michx.) and Arabidopsis (Arabidopsis thaliana (L.) Heynh), to decrease contents of the 4-O-methyl glucuronopyranose acid (mGlcA) substituent of xylan, to elucidate mGlcA's functions.

    The enzyme affected the content of aliphatic insoluble cell wall components having composition similar to suberin, which required mGlcA for binding to cell walls. Such suberin-like compounds have been previously identified in decayed wood, but here, we show their presence in healthy wood of both hardwood and softwood species. By contrast, γ-ester bonds between mGlcA and lignin were insensitive to cell wall-localized α-glucuronidase, supporting the intracellular formation of these bonds.

    These findings challenge the current view of the wood cell wall composition and reveal a novel function of mGlcA substituent of xylan in fastening of suberin-like compounds to cell wall. They also suggest an intracellular initiation of lignin–carbohydrate complex assembly.

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  • 27. Ding, Jihua
    et al.
    Böhlenius, Henrik
    Rühl, Mark Georg
    Chen, Peng
    Sane, Shashank
    Zambrano, Jose A.
    Zheng, Bo
    Nilsson, Ove
    Eriksson, Maria E.
    Umeå University, Faculty of Science and Technology, Department of Plant Physiology. Umeå University, Faculty of Science and Technology, Umeå Plant Science Centre (UPSC).
    GIGANTEA-like genes control seasonal growth cessation in Populus2018In: New Phytologist, ISSN 0028-646X, E-ISSN 1469-8137, Vol. 218, no 4, p. 1491-1503Article in journal (Refereed)
    Abstract [en]

    Survival of trees growing in temperate zones requires cycling between active growth and dormancy. This involves growth cessation in the autumn triggered by a photoperiod shorter than the critical day length. Variations in GIGANTEA (GI)-like genes have been associated with phenology in a range of different tree species, but characterization of the functions of these genes in the process is still lacking. We describe the identification of the Populus orthologs of GI and their critical role in short-day-induced growth cessation. Using ectopic expression and silencing, gene expression analysis, protein interaction and chromatin immunoprecipitation experiments, we show that PttGIs are likely to act in a complex with PttFKF1s (FLAVIN-BINDING, KELCH REPEAT, F-BOX 1) and PttCDFs (CYCLING DOF FACTOR) to control the expression of PttFT2, the key gene regulating short-day-induced growth cessation in Populus. In contrast to Arabidopsis, in which the GI-CONSTANS (CO)-FLOWERING LOCUS T (FT) regulon is a crucial day-length sensor for flowering time, our study suggests that, in Populus, PttCO-independent regulation of PttFT2 by PttGI is more important in the photoperiodic control of growth cessation and bud set.

  • 28. Dominguez, Pia Guadalupe
    et al.
    Donev, Evgeniy
    Derba-Maceluch, Marta
    Bünder, Anne
    Hedenström, Mattias
    Umeå University, Faculty of Science and Technology, Department of Chemistry.
    Tomásková, Ivana
    Mellerowicz, Ewa J.
    Niittylä, Totte
    Sucrose synthase determines carbon allocation in developing wood and alters carbon flow at the whole tree level in aspen2021In: New Phytologist, ISSN 0028-646X, E-ISSN 1469-8137, Vol. 229, no 1, p. 186-198Article in journal (Refereed)
    Abstract [en]

    Despite the ecological and industrial importance of biomass accumulation in wood, the control of carbon (C) allocation to this tissue and to other tree tissues remain poorly understood. We studied sucrose synthase (SUS) to clarify its role in biomass formation and C metabolism at the whole tree level in hybrid aspen (Populus tremula x tremuloides). To this end, we analysed source leaves, phloem, developing wood, and roots ofSUSRNAitrees using a combination of metabolite profiling, 13CO2 pulse labelling experiments, and long-term field experiments. The glasshouse grownSUSRNAitrees exhibited a mild stem phenotype together with a reduction in wood total C. The 13CO2 pulse labelling experiments showed an alteration in the C flow in all the analysed tissues, indicating that SUS affects C metabolism at the whole tree level. This was confirmed when theSUSRNAitrees were grown in the field over a 5-yr period; their stem height, diameter and biomass were substantially reduced. These results establish that SUS influences C allocation to developing wood, and that it affects C metabolism at the whole tree level.

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  • 29. Doyle, Siamsa M.
    et al.
    Rigal, Adeline
    Grones, Peter
    Karady, Michal
    Barange, Deepak Kumar
    Umeå University, Faculty of Science and Technology, Department of Chemistry.
    Majda, Mateusz
    Parizkova, Barbora
    Karampelias, Michael
    Zwiewka, Marta
    Pencik, Ales
    Umeå University, Faculty of Science and Technology, Department of Chemistry.
    Almqvist, Fredrik
    Ljung, Karin
    Novak, Ondrej
    Umeå University, Faculty of Science and Technology, Department of Chemistry.
    Robert, Stephanie
    A role for the auxin precursor anthranilic acid in root gravitropism via regulation of PIN‐FORMED protein polarity and relocalisation in Arabidopsis2019In: New Phytologist, ISSN 0028-646X, E-ISSN 1469-8137, Vol. 223, no 3, p. 1420-1432Article in journal (Refereed)
    Abstract [en]

    Distribution of auxin within plant tissues is of great importance for developmental plasticity, including root gravitropic growth. Auxin flow is directed by the subcellular polar distribution and dynamic relocalisation of auxin transporters such as the PIN‐FORMED (PIN) efflux carriers, which can be influenced by the main natural plant auxin indole‐3‐acetic acid (IAA). Anthranilic acid (AA) is an important early precursor of IAA and previously published studies with AA analogues have suggested that AA may also regulate PIN localisation.

    Using Arabidopsis thaliana as a model species, we studied an AA‐deficient mutant displaying agravitropic root growth, treated seedlings with AA and AA analogues and transformed lines to over‐produce AA while inhibiting its conversion to downstream IAA precursors.

    We showed that AA rescues root gravitropic growth in the AA‐deficient mutant at concentrations that do not rescue IAA levels. Overproduction of AA affects root gravitropism without affecting IAA levels. Treatments with, or deficiency in, AA result in defects in PIN polarity and gravistimulus‐induced PIN relocalisation in root cells.

    Our results revealed a previously unknown role for AA in the regulation of PIN subcellular localisation and dynamics involved in root gravitropism, which is independent of its better known role in IAA biosynthesis.

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  • 30.
    El Arbi, Nabila
    et al.
    Umeå University, Faculty of Science and Technology, Department of Plant Physiology. Umeå University, Faculty of Science and Technology, Umeå Plant Science Centre (UPSC).
    Muniz Nardeli, Sarah
    Umeå University, Faculty of Science and Technology, Department of Plant Physiology. Umeå University, Faculty of Science and Technology, Umeå Plant Science Centre (UPSC). Department of Plant Biology, Linnean Center for Plant Biology, Swedish University of Agricultural Sciences, Uppsala, Sweden.
    Šimura, Jan
    Department of Forest Genetics and Plant Physiology, Umeå Plant Science Centre, Swedish University of Agricultural Sciences, Umeå, Sweden.
    Ljung, Karin
    Department of Forest Genetics and Plant Physiology, Umeå Plant Science Centre, Swedish University of Agricultural Sciences, Umeå, Sweden.
    Schmid, Markus
    Umeå University, Faculty of Science and Technology, Department of Plant Physiology. Umeå University, Faculty of Science and Technology, Umeå Plant Science Centre (UPSC). Department of Plant Biology, Linnean Center for Plant Biology, Swedish University of Agricultural Sciences, Uppsala, Sweden.
    The Arabidopsis splicing factor PORCUPINE/SmE1 orchestrates temperature-dependent root development via auxin homeostasis maintenance2024In: New Phytologist, ISSN 0028-646X, E-ISSN 1469-8137, Vol. 244, no 4, p. 1408-1421Article in journal (Refereed)
    Abstract [en]
    • Appropriate abiotic stress response is pivotal for plant survival and makes use of multiple signaling molecules and phytohormones to achieve specific and fast molecular adjustments. A multitude of studies has highlighted the role of alternative splicing in response to abiotic stress, including temperature, emphasizing the role of transcriptional regulation for stress response. Here we investigated the role of the core-splicing factor PORCUPINE (PCP) on temperature-dependent root development.
    • We used marker lines and transcriptomic analyses to study the expression profiles of meristematic regulators and mitotic markers, and chemical treatments, as well as root hormone profiling to assess the effect of auxin signaling.
    • The loss of PCP significantly alters RAM architecture in a temperature-dependent manner. Our results indicate that PCP modulates the expression of central meristematic regulators and is required to maintain appropriate levels of auxin in the RAM.
    • We conclude that alternative pre-mRNA splicing is sensitive to moderate temperature fluctuations and contributes to root meristem maintenance, possibly through the regulation of phytohormone homeostasis and meristematic activity.
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  • 31.
    Eriksson, Maria E.
    et al.
    Umeå University, Faculty of Science and Technology, Department of Plant Physiology. Umeå University, Faculty of Science and Technology, Umeå Plant Science Centre (UPSC).
    Hoffman, Daniel
    Kaduk, Mateusz
    Mauriat, Melanie
    Moritz, Thomas
    Transgenic hybrid aspen trees with increased gibberellin (GA) concentrations suggest that GA acts in parallel with FLOWERING LOCUS T2 to control shoot elongation2015In: New Phytologist, ISSN 0028-646X, E-ISSN 1469-8137, Vol. 205, no 3, p. 1288-1295Article in journal (Refereed)
    Abstract [en]

    Bioactive gibberellins (GAs) have been implicated in short day (SD)-induced growth cessation in Populus, because exogenous applications of bioactive GAs to hybrid aspens (Populus tremulaxtremuloides) under SD conditions delay growth cessation. However, this effect diminishes with time, suggesting that plants may cease growth following exposure to SDs due to a reduction in sensitivity to GAs.

    In order to validate and further explore the role of GAs in growth cessation, we perturbed GA biosynthesis or signalling in hybrid aspen plants by overexpressing AtGA20ox1, AtGA2ox2 and PttGID1.3 (encoding GA biosynthesis enzymes and a GA receptor).

    We found trees with elevated concentrations of bioactive GA, due to overexpression of AtGA20ox1, continued to grow in SD conditions and were insensitive to the level of FLOWERING LOCUS T2 (FT2) expression. As transgenic plants overexpressing the PttGID1.3 GA receptor responded in a wild-type (WT) manner to SD conditions, this insensitivity did not result from limited receptor availability.

    As high concentrations of bioactive GA during SD conditions were sufficient to sustain shoot elongation growth in hybrid aspen trees, independent of FT2 expression levels, we conclude elongation growth in trees is regulated by both GA- and long day-responsive pathways, similar to the regulation of flowering in Arabidopsis thaliana.

  • 32.
    Fang, Chao
    et al.
    Research Center for Global Changes and Ecosystem Carbon Sequestration & Mitigation, School of Applied Meteorology, Nanjing University of Information Science and Technology, Nanjing, China; PLECO (Plants and Ecosystems), Department of Biology, University of Antwerp, Universiteitsplein 1, Wilrijk, Belgium.
    Verbrigghe, Niel
    Flanders Research Institute for Agriculture, Fisheries and Food, Caritasstraat 39, Melle, Belgium.
    Sigurdsson, Bjarni D.
    Agricultural University of Iceland, Hvanneyri, Borgarnes, Iceland.
    Ostonen, Ivika
    Institute of Ecology and Earth Sciences, University of Tartu, Tartu, Estonia.
    Leblans, Niki I.W.
    Umeå University, Faculty of Science and Technology, Department of Ecology and Environmental Sciences.
    Marañón-Jiménez, Sara
    CREAF, Cerdanyola del Vallès, Catalonia, Barcelona, Spain; CSIC, Global Ecology Unit CREAF-CSIC-UAB, Bellaterra, Catalonia, Barcelona, Spain; Universitat Autònoma de Barcelona, Cerdanyola del Vallès, Spain.
    Fuchslueger, Lucia
    Centre for Microbiology and Environmental Systems Science, University of Vienna, Djerassiplatz 1, Vienna, Austria.
    Sigurðsson, Páll
    Agricultural University of Iceland, Hvanneyri, Borgarnes, Iceland.
    Meeran, Kathiravan
    Department of Ecology, University of Innsbruck, Innsbruck, Austria.
    Portillo-Estrada, Miguel
    PLECO (Plants and Ecosystems), Department of Biology, University of Antwerp, Universiteitsplein 1, Wilrijk, Belgium.
    Verbruggen, Erik
    PLECO (Plants and Ecosystems), Department of Biology, University of Antwerp, Universiteitsplein 1, Wilrijk, Belgium.
    Richter, Andreas
    Centre for Microbiology and Environmental Systems Science, University of Vienna, Djerassiplatz 1, Vienna, Austria.
    Sardans, Jordi
    CREAF, Cerdanyola del Vallès, Catalonia, Barcelona, Spain; CSIC, Global Ecology Unit CREAF-CSIC-UAB, Bellaterra, Catalonia, Barcelona, Spain.
    Peñuelas, Josep
    CREAF, Cerdanyola del Vallès, Catalonia, Barcelona, Spain; CSIC, Global Ecology Unit CREAF-CSIC-UAB, Bellaterra, Catalonia, Barcelona, Spain.
    Bahn, Michael
    Department of Ecology, University of Innsbruck, Innsbruck, Austria.
    Vicca, Sara
    PLECO (Plants and Ecosystems), Department of Biology, University of Antwerp, Universiteitsplein 1, Wilrijk, Belgium.
    Janssens, Ivan A.
    PLECO (Plants and Ecosystems), Department of Biology, University of Antwerp, Universiteitsplein 1, Wilrijk, Belgium.
    Decadal soil warming decreased vascular plant above and belowground production in a subarctic grassland by inducing nitrogen limitation2023In: New Phytologist, ISSN 0028-646X, E-ISSN 1469-8137, Vol. 240, no 2, p. 565-576Article in journal (Refereed)
    Abstract [en]
    • Below and aboveground vegetation dynamics are crucial in understanding how climate warming may affect terrestrial ecosystem carbon cycling. In contrast to aboveground biomass, the response of belowground biomass to long-term warming has been poorly studied.
    • Here, we characterized the impacts of decadal geothermal warming at two levels (on average +3.3°C and +7.9°C) on below and aboveground plant biomass stocks and production in a subarctic grassland.
    • Soil warming did not change standing root biomass and even decreased fine root production and reduced aboveground biomass and production. Decadal soil warming also did not significantly alter the root–shoot ratio. The linear stepwise regression model suggested that following 10 yr of soil warming, temperature was no longer the direct driver of these responses, but losses of soil N were. Soil N losses, due to warming-induced decreases in organic matter and water retention capacity, were identified as key driver of the decreased above and belowground production. The reduction in fine root production was accompanied by thinner roots with increased specific root area.
    • These results indicate that after a decade of soil warming, plant productivity in the studied subarctic grassland was affected by soil warming mainly by the reduction in soil N.
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  • 33. Felten, Judith
    et al.
    Vahala, Jorma
    Love, Jonathan
    Gorzsás, András
    Umeå University, Faculty of Science and Technology, Department of Chemistry.
    Ruggeberg, Markus
    Delhomme, Nicolas
    Lesniewska, Joanna
    Kangasjarvi, Jaakko
    Hvidsten, Torgeir R.
    Umeå University, Faculty of Science and Technology, Umeå Plant Science Centre (UPSC). Faculty of Chemistry, Biotechnology and Food Science, Norwegian University of Life Sciences,Ås, Norway.
    Mellerowicz, Ewa J.
    Sundberg, Bjorn
    Ethylene signaling induces gelatinous layers with typical features of tension wood in hybrid aspen2018In: New Phytologist, ISSN 0028-646X, E-ISSN 1469-8137, Vol. 218, no 3, p. 999-1014Article in journal (Refereed)
    Abstract [en]

    The phytohormone ethylene impacts secondary stem growth in plants by stimulating cambial activity, xylem development and fiber over vessel formation. We report the effect of ethylene on secondary cell wall formation and the molecular connection between ethylene signaling and wood formation. We applied exogenous ethylene or its precursor 1-aminocyclopropane-1-carboxylic acid (ACC) to wild-type and ethylene-insensitive hybrid aspen trees (Populus tremulaxtremuloides) and studied secondary cell wall anatomy, chemistry and ultrastructure. We furthermore analyzed the transcriptome (RNA Seq) after ACC application to wild-type and ethylene-insensitive trees. We demonstrate that ACC and ethylene induce gelatinous layers (G-layers) and alter the fiber cell wall cellulose microfibril angle. G-layers are tertiary wall layers rich in cellulose, typically found in tension wood of aspen trees. A vast majority of transcripts affected by ACC are downstream of ethylene perception and include a large number of transcription factors (TFs). Motif-analyses reveal potential connections between ethylene TFs (Ethylene Response Factors (ERFs), ETHYLENE INSENSITIVE 3/ETHYLENE INSENSITIVE3-LIKE1 (EIN3/EIL1)) and wood formation. G-layer formation upon ethylene application suggests that the increase in ethylene biosynthesis observed during tension wood formation is important for its formation. Ethylene-regulated TFs of the ERF and EIN3/EIL1 type could transmit the ethylene signal.

  • 34.
    Frenkel, Martin
    et al.
    Umeå University, Faculty of Science and Technology, Department of Ecology and Environmental Sciences.
    Johansson Jänkänpää, Hanna
    Umeå University, Faculty of Science and Technology, Umeå Plant Science Centre (UPSC).
    Moen, Jon
    Umeå University, Faculty of Science and Technology, Department of Ecology and Environmental Sciences.
    Jansson, Stefan
    Umeå University, Faculty of Science and Technology, Umeå Plant Science Centre (UPSC).
    An illustrated gardener's guide to transgenic Arabidopsis field experiments2008In: New Phytologist, ISSN 0028-646X, E-ISSN 1469-8137, Vol. 180, no 2, p. 545-555Article in journal (Refereed)
    Abstract [en]

    Field studies with transgenic Arabidopsislines have been performed over 8 yr, to better understand the influence that certain genes have on plant performance. Many (if not most) plant phenotypes cannot be observed under the near constant, low-stress conditions in growth chambers, making field experiments necessary. However, there are challenges in performing such experiments: permission must be obtained and regulations obeyed, the profound influence of uncontrollable biotic and abiotic factors has to be considered, and experimental design has to be strictly controlled.

    The aim here is to provide inspiration and guidelines for researchers who are not used to setting up such experiments, allowing others to learn from our mistakes. This is believed to be the first example of a ‘manual’ for field experiments with transgenic Arabidopsisplants. Many of the challenges encountered are common for all field experiments, and many researchers from ecological backgrounds are skilled in such methods. There is huge potential in combining the detailed mechanistic understanding of molecular biologists with ecologists’ expertise in examining plant performance under field conditions, and it is suggested that more interdisciplinary collaborations will open up new scientific avenues to aid analyses of the roles of genetic and physiological variation in natural systems.

  • 35. Gauslaa, Yngvar
    et al.
    Palmqvist, Kristin
    Umeå University, Faculty of Science and Technology, Department of Ecology and Environmental Sciences.
    Solhaug, Knut Asbjørn
    Hilmo, Olga
    Holien, Håkon
    Nybakken, Line
    Ohlson, Mikael
    Size-dependent growth of two old-growth associated macrolichen species2009In: New Phytologist, ISSN 0028-646X, E-ISSN 1469-8137, Vol. 181, no 3, p. 683-692Article in journal (Refereed)
    Abstract [en]

    Relationships between thallus size and growth variables were analysed for the foliose Lobaria pulmonaria and the pendulous Usnea longissima with the aim of elucidating their morphogenesis and the factors determining thallus area (A) versus biomass (dry weight (DW) gain. Size and growth data originated from a factorial transplantation experiment that included three boreal climate zones (Atlantic, suboceanic and continental), each with three successional forest stands (clear-cut, young and old). When A was replaced by the estimated photobiont layer area in an area-DW scatterplot including all thalli (n = 1080), the two separate species clusters merged into one, suggesting similar allocation patterns between photobionts and mycobionts across growth forms. During transplantation, stand-specific water availability boosted area gain in foliose transplants, consistent with a positive role of water in fungal expansion. In pendulous lichens, A gain greatly exceeded DW gain, particularly in small transplants. The A gain in U. longissima increased with increasing DW:A ratio, consistent with a reallocation of carbon, presumably mobilized from the dense central chord. Pendulous lichens with cylindrical photobiont layers harvest light from all sides. Rapid and flexible three-dimensional A gain allows the colonization of spaces between canopy branches to utilize temporary windows of light in a growing canopy. Foliose lichens with a two-dimensional photobiont layer have more coupled A and DW gains.

  • 36. Grimberg, Åsa
    et al.
    Lager, Ida
    Street, Nathaniel
    Umeå University, Faculty of Science and Technology, Department of Plant Physiology. Umeå University, Faculty of Science and Technology, Umeå Plant Science Centre (UPSC).
    Robinson, Kathryn M
    Umeå University, Faculty of Science and Technology, Department of Plant Physiology. Umeå University, Faculty of Science and Technology, Umeå Plant Science Centre (UPSC).
    Marttila, Salla
    Mähler, Niklas
    Umeå University, Faculty of Science and Technology, Umeå Plant Science Centre (UPSC). Umeå University, Faculty of Science and Technology, Department of Plant Physiology.
    Ingvarsson, Pär K.
    Bhalerao, Rishikesh P.
    Storage lipid accumulation is controlled by photoperiodic signal acting via regulators of growth cessation and dormancy in hybrid aspen2018In: New Phytologist, ISSN 0028-646X, E-ISSN 1469-8137, Vol. 219, no 2, p. 619-630Article in journal (Refereed)
    Abstract [en]

    The signalling pathways that control seasonal modulation of carbon metabolism in perennial plants are poorly understood. Using genetic, metabolic and natural variation approaches, we identify factors mediating photoperiodic control of storage lipid accumulation in the model tree hybrid aspen (Populus tremula x tremuloides). We characterized lipid accumulation in transgenic hybrid aspen with impaired photoperiodic and hormonal responses. Genome-wide association mapping was performed in Swedish aspen (P.tremula) genotypes to determine genetic loci associated with genotype variation in lipid content. Our data show that the storage lipid triacylglycerol (TAG) accumulates in cambial meristem and pith rays of aspen in response to photoperiodic signal controlling growth cessation and dormancy induction. We show that photoperiodic control of TAG accumulation is mediated by the FLOWERING LOCUS T/CONSTANS module, which also controls the induction of growth cessation. Hormonal and chromatin remodelling pathways also contribute to TAG accumulation by photoperiodic signal. Natural variation exists in lipid accumulation that is controlled by input from multiple loci. Our data shed light on how the control of storage metabolism is temporally coordinated with growth cessation and dormancy by photoperiodic signal, and reveals that storage lipid accumulation between seeds and perennating organs of trees may involve distinct regulatory circuits.

  • 37.
    Grönlund, Andreas
    et al.
    Umeå University, Faculty of Science and Technology, Department of Plant Physiology.
    Bhalerao, Rishikesh P
    Umeå University, Faculty of Science and Technology, Umeå Plant Science Centre (UPSC).
    Karlsson, Jan
    Umeå University, Faculty of Science and Technology, Department of Plant Physiology. Umeå University, Faculty of Science and Technology, Umeå Plant Science Centre (UPSC).
    Modular gene expression in Poplar: a multilayer network approach2009In: New Phytologist, ISSN 0028-646X, E-ISSN 1469-8137, Vol. 181, no 2, p. 315-322Article in journal (Refereed)
    Abstract [en]

    * By applying a multilayer network approach to an extensive set of Poplar microarray data, a genome-wide coexpression network has been detected and explored.

    * Multilayer networks were generated from minimum spanning trees (MSTs) using Kruskal's algorithm from random jack-knife resamplings of half of the full data set. The final network is obtained from the union of all the generated MSTs.

    * The gene expression correlations display a highly clustered topology, which is more pronounced when introducing links appearing in relatively few of the generated MSTs. The network also reveals a modular architecture, reflecting functional groups with relatively frequent gene-to-gene communication. Furthermore, the observed modular structure overlaps with different gene activities in different tissues, and closely related tissues show similar over- and/or under-expression patterns at the modular scale.

    * It is shown that including links that appear in a few of the generated MSTs increases the information quality of the network. In other words, a link may be 'weak' because it reflects rare signaling events rather than merely a signal weakened by noise. The method allows, from comparisons of random 'null networks', tuning to maximize the information obtainable.

  • 38.
    Harrison, Sandy P.
    et al.
    Department of Geography and Environmental Science, University of Reading, Reading, United Kingdom; Ministry of Education Key Laboratory for Earth System Modeling, Department of Earth System Science, Tsinghua University, Beijing, China.
    Cramer, Wolfgang
    Institut Méditerranéen de Biodiversité et d’Ecologie Marine et Continentale, Aix Marseille Université, CNRS, IRD, Avignon Université, Technopôle Arbois-Méditerranée, Aix-en-Provence Cedex 04, France.
    Franklin, Oskar
    International Institute for Applied Systems Analysis, Schlossplatz 1, Laxenburg, Austria; Department of Forest Ecology and Management, Swedish University of Agricultural Sciences, Umeå, Sweden.
    Prentice, Iain Colin
    Ministry of Education Key Laboratory for Earth System Modeling, Department of Earth System Science, Tsinghua University, Beijing, China; Department of Life Sciences, Imperial College London, Silwood Park Campus, Buckhurst Road, Ascot, United Kingdom; Department of Biological Sciences, Macquarie University, NSW, North Ryde, Australia.
    Wang, Han
    Ministry of Education Key Laboratory for Earth System Modeling, Department of Earth System Science, Tsinghua University, Beijing, China.
    Brännström, Åke
    Umeå University, Faculty of Science and Technology, Department of Mathematics and Mathematical Statistics. International Institute for Applied Systems Analysis, Schlossplatz 1, Laxenburg, Austria.
    de Boer, Hugo
    Copernicus Institute of Sustainable Development, Environmental Sciences, Faculty of Geosciences, Utrecht University, Vening Meinesz Building, Princetonlaan 8a, Utrecht, Netherlands.
    Dieckmann, Ulf
    International Institute for Applied Systems Analysis, Schlossplatz 1, Laxenburg, Austria; Department of Evolutionary Studies of Biosystems, The Graduate University for Advanced Studies (Sokendai), Kanagawa, Hayama, Japan.
    Joshi, Jaideep
    International Institute for Applied Systems Analysis, Schlossplatz 1, Laxenburg, Austria.
    Keenan, Trevor F.
    Climate and Ecosystem Sciences Division, Lawrence Berkeley National Laboratory, 1 Cyclotron Road, CA, Berkeley, United States; Department of Environmental Science, Policy and Management, University of California Berkeley, CA, Berkeley, United States.
    Lavergne, Aliénor
    Department of Physics, Imperial College London, South Kensington Campus, London, United Kingdom.
    Manzoni, Stefano
    Department of Physical Geography and Bolin Centre for Climate Research, Stockholm University, SE-106 91, Stockholm, Sweden.
    Mengoli, Giulia
    Department of Life Sciences, Imperial College London, Silwood Park Campus, Buckhurst Road, Ascot, United Kingdom.
    Morfopoulos, Catherine
    Department of Life Sciences, Imperial College London, Silwood Park Campus, Buckhurst Road, Ascot, United Kingdom.
    Peñuelas, Josep
    CSIC, Global Ecology, CREAF-CSIC-UAB, Bellaterra, Catalonia, Barcelona, Spain; CREAF, Cerdanyola del Valles, Catalonia, Barcelona, Spain.
    Pietsch, Stephan
    International Institute for Applied Systems Analysis, Schlossplatz 1, Laxenburg, Austria; BOKU - University of Life Sciences and Natural Resources, Gregor-Medel-Strasse 33, Vienna, Austria.
    Rebel, Karin T.
    Copernicus Institute of Sustainable Development, Environmental Sciences, Faculty of Geosciences, Utrecht University, Vening Meinesz Building, Princetonlaan 8a, Utrecht, Netherlands.
    Ryu, Youngryel
    Department of Landscape Architecture and Rural Systems Engineering, Seoul National University, Seoul, South Korea.
    Smith, Nicholas G.
    Department of Biological Sciences, Texas Tech University, 2901 Main Street, TX, Lubbock, United States.
    Stocker, Benjamin D.
    Department of Environmental System Science, ETH, Universitätstrasse 2, Zürich, Switzerland; Swiss Federal Institute for Forest, Snow and Landscape Research WSL, Zrcherstrasse 111, Birmensdorf, Switzerland.
    Wright, Ian J.
    Department of Biological Sciences, Macquarie University, NSW, North Ryde, Australia.
    Eco-evolutionary optimality as a means to improve vegetation and land-surface models2021In: New Phytologist, ISSN 0028-646X, E-ISSN 1469-8137, Vol. 231, no 6, p. 2125-2141Article, review/survey (Refereed)
    Abstract [en]

    Global vegetation and land-surface models embody interdisciplinary scientific understanding of the behaviour of plants and ecosystems, and are indispensable to project the impacts of environmental change on vegetation and the interactions between vegetation and climate. However, systematic errors and persistently large differences among carbon and water cycle projections by different models highlight the limitations of current process formulations. In this review, focusing on core plant functions in the terrestrial carbon and water cycles, we show how unifying hypotheses derived from eco-evolutionary optimality (EEO) principles can provide novel, parameter-sparse representations of plant and vegetation processes. We present case studies that demonstrate how EEO generates parsimonious representations of core, leaf-level processes that are individually testable and supported by evidence. EEO approaches to photosynthesis and primary production, dark respiration and stomatal behaviour are ripe for implementation in global models. EEO approaches to other important traits, including the leaf economics spectrum and applications of EEO at the community level are active research areas. Independently tested modules emerging from EEO studies could profitably be integrated into modelling frameworks that account for the multiple time scales on which plants and plant communities adjust to environmental change.

  • 39.
    Hernández-Verdeja, Tamara
    et al.
    Umeå University, Faculty of Science and Technology, Department of Plant Physiology. Umeå University, Faculty of Science and Technology, Umeå Plant Science Centre (UPSC).
    Vuorijoki, Linda
    Umeå University, Faculty of Science and Technology, Department of Plant Physiology. Umeå University, Faculty of Science and Technology, Umeå Plant Science Centre (UPSC).
    Jin, Xu
    Umeå University, Faculty of Science and Technology, Department of Plant Physiology. Umeå University, Faculty of Science and Technology, Umeå Plant Science Centre (UPSC).
    Vergara, Alexander
    Umeå University, Faculty of Science and Technology, Department of Plant Physiology. Umeå University, Faculty of Science and Technology, Umeå Plant Science Centre (UPSC).
    Dubreuil, Carole
    Umeå University, Faculty of Science and Technology, Department of Plant Physiology. Umeå University, Faculty of Science and Technology, Umeå Plant Science Centre (UPSC).
    Strand, Åsa
    Umeå University, Faculty of Science and Technology, Department of Plant Physiology. Umeå University, Faculty of Science and Technology, Umeå Plant Science Centre (UPSC).
    GENOMES UNCOUPLED1 plays a key role during the de-etiolation process in Arabidopsis2022In: New Phytologist, ISSN 0028-646X, E-ISSN 1469-8137, Vol. 235, no 1, p. 188-203Article in journal (Refereed)
    Abstract [en]
    • One of the most dramatic challenges in the life of a plant occurs when the seedling emerges from the soil and exposure to light triggers expression of genes required for establishment of photosynthesis.
    • This process needs to be tightly regulated, as premature accumulation of light-harvesting proteins and photoreactive Chl precursors causes oxidative damage when the seedling is first exposed to light. Photosynthesis genes are encoded by both nuclear and plastid genomes, and to establish the required level of control, plastid-to-nucleus (retrograde) signalling is necessary to ensure correct gene expression.
    • We herein show that a negative GENOMES UNCOUPLED1 (GUN1)-mediated retrograde signal restricts chloroplast development in darkness and during early light response by regulating the transcription of several critical transcription factors linked to light response, photomorphogenesis, and chloroplast development, and consequently their downstream target genes in Arabidopsis.
    • Thus, the plastids play an essential role during skotomorphogenesis and the early light response, and GUN1 acts as a safeguard during the critical step of seedling emergence from darkness.
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  • 40. Hogberg, Mona N.
    et al.
    Briones, Maria J. I.
    Keel, Sonja G.
    Metcalfe, Daniel B.
    Campbell, Catherine
    Umeå University, Faculty of Science and Technology, Umeå Plant Science Centre (UPSC).
    Midwood, Andrew J.
    Thornton, Barry
    Hurry, Vaughan
    Umeå University, Faculty of Science and Technology, Department of Plant Physiology. Umeå University, Faculty of Science and Technology, Umeå Plant Science Centre (UPSC).
    Linder, Sune
    Nasholm, Torgny
    Umeå University, Faculty of Science and Technology, Umeå Plant Science Centre (UPSC).
    Hogberg, Peter
    Quantification of effects of season and nitrogen supply on tree below-ground carbon transfer to ectomycorrhizal fungi and other soil organisms in a boreal pine forest2010In: New Phytologist, ISSN 0028-646X, E-ISSN 1469-8137, Vol. 187, no 2, p. 485-493Article in journal (Refereed)
    Abstract [en]

    P>The flux of carbon from tree photosynthesis through roots to ectomycorrhizal (ECM) fungi and other soil organisms is assumed to vary with season and with edaphic factors such as nitrogen availability, but these effects have not been quantified directly in the field. To address this deficiency, we conducted high temporal-resolution tracing of 13C from canopy photosynthesis to different groups of soil organisms in a young boreal Pinus sylvestris forest. There was a 500% higher below-ground allocation of plant C in the late (August) season compared with the early season (June). Labelled C was primarily found in fungal fatty acid biomarkers (and rarely in bacterial biomarkers), and in Collembola, but not in Acari and Enchytraeidae. The production of sporocarps of ECM fungi was totally dependent on allocation of recent photosynthate in the late season. There was no short-term (2 wk) effect of additions of N to the soil, but after 1 yr, there was a 60% reduction of below-ground C allocation to soil biota. Thus, organisms in forest soils, and their roles in ecosystem functions, appear highly sensitive to plant physiological responses to two major aspects of global change: changes in seasonal weather patterns and N eutrophication.

  • 41.
    HUSSDANELL, K
    Umeå University, Faculty of Science and Technology, Department of Plant Physiology.
    NITROGEN-FIXATION AND BIOMASS PRODUCTION IN CLONES OF ALNUS-INCANA1980In: New Phytologist, ISSN 0028-646X, E-ISSN 1469-8137, Vol. 85, no 4, p. 503-511Article in journal (Refereed)
  • 42. Högberg, Peter
    et al.
    Högberg, M. N.
    Göttlicher, S. G.
    Betson, N. R.
    Keel, S. G.
    Metcalfe, D. B.
    Campbell, Catherine
    Umeå University, Faculty of Science and Technology, Umeå Plant Science Centre (UPSC).
    Schindlbacher, A.
    Hurry, Vaughan
    Umeå University, Faculty of Science and Technology, Department of Plant Physiology. Umeå University, Faculty of Science and Technology, Umeå Plant Science Centre (UPSC).
    Lundmark, Thomas
    Linder, Sune
    Näsholm, Torgny
    Umeå University, Faculty of Science and Technology, Umeå Plant Science Centre (UPSC).
    High temporal resolution tracing of photosynthate carbon from the tree canopy to forest soil microorganisms2008In: New Phytologist, ISSN 0028-646X, E-ISSN 1469-8137, Vol. 177, no 1, p. 220-228Article in journal (Refereed)
    Abstract [en]

    • Half of the biological activity in forest soils is supported by recent tree photosynthate, but no study has traced in detail this flux of carbon from the canopy to soil microorganisms in the field.

    • Using 13CO2, we pulse-labelled over 1.5 h a 50-m2 patch of 4-m-tall boreal Pinus sylvestris forest in a 200-m3 chamber.

    • Tracer levels peaked after 24 h in soluble carbohydrates in the phloem at a height of 0.3 m, after 2–4 d in soil respiratory efflux, after 4–7 d in ectomycorrhizal roots, and after 2–4 d in soil microbial cytoplasm. Carbon in the active pool in needles, in soluble carbohydrates in phloem and in soil respiratory efflux had half-lives of 22, 17 and 35 h, respectively. Carbon in soil microbial cytoplasm had a half-life of 280 h, while the carbon in ectomycorrhizal root tips turned over much more slowly. Simultaneous labelling of the soil with showed that the ectomycorrhizal roots, which were the strongest sinks for photosynthate, were also the most active sinks for soil nitrogen.

    • These observations highlight the close temporal coupling between tree canopy photosynthesis and a significant fraction of soil activity in forests.

  • 43.
    Ingvarsson, Pär K.
    et al.
    Umeå University, Faculty of Science and Technology, Department of Ecology and Environmental Sciences. Umeå University, Faculty of Science and Technology, Umeå Plant Science Centre (UPSC).
    Hvidsten, Torgeir R.
    Umeå University, Faculty of Science and Technology, Department of Plant Physiology. Umeå University, Faculty of Science and Technology, Umeå Plant Science Centre (UPSC). Department of Chemistry, Biotechnology and Food Science, Norwegian University of Life Sciences, 1432,As, Norway.
    Street, Nathaniel R.
    Umeå University, Faculty of Science and Technology, Department of Plant Physiology. Umeå University, Faculty of Science and Technology, Umeå Plant Science Centre (UPSC).
    Towards integration of population and comparative genomics in forest trees2016In: New Phytologist, ISSN 0028-646X, E-ISSN 1469-8137, Vol. 212, no 2, p. 338-344Article, review/survey (Refereed)
    Abstract [en]

    The past decade saw the initiation of an ongoing revolution in sequencing technologies that is transforming all fields of biology. This has been driven by the advent and widespread availability of high-throughput, massively parallel short-read sequencing (MPS) platforms. These technologies have enabled previously unimaginable studies, including draft assemblies of the massive genomes of coniferous species and population-scale resequencing. Transcriptomics studies have likewise been transformed, with RNA-sequencing enabling studies in nonmodel organisms, the discovery of previously unannotated genes (novel transcripts), entirely new classes of RNAs and previously unknown regulatory mechanisms. Here we touch upon current developments in the areas of genome assembly, comparative regulomics and population genetics as they relate to studies of forest tree species.

  • 44.
    Ingvarsson, Pär K
    et al.
    Umeå University, Faculty of Science and Technology, Department of Ecology and Environmental Sciences.
    Street, Nathaniel R
    Umeå University, Faculty of Science and Technology, Department of Plant Physiology. Umeå University, Faculty of Science and Technology, Umeå Plant Science Centre (UPSC).
    Association genetics of complex traits in plants2011In: New Phytologist, ISSN 0028-646X, E-ISSN 1469-8137, Vol. 189, no 4, p. 909-922Article in journal (Refereed)
    Abstract [en]

    Association mapping is rapidly becoming the main method for dissecting the genetic architecture of complex traits in plants. Currently most association mapping studies in plants are preformed using sets of genes selected to be putative candidates for the trait of interest, but rapid developments in genomics will allow for genome-wide mapping in virtually any plant species in the near future. As the costs for genotyping are decreasing, the focus has shifted towards phenotyping. In plants, clonal replication and/or inbred lines allows for replicated phenotyping under many different environmental conditions. Reduced sequencing costs will increase the number of studies that use RNA sequencing data to perform expression quantitative trait locus (eQTL) mapping, which will increase our knowledge of how gene expression variation contributes to phenotypic variation. Current population sizes used in association mapping studies are modest in size and need to be greatly increased if mutations explaining less than a few per cent of the phenotypic variation are to be detected. Association mapping has started to yield insights into the genetic architecture of complex traits in plants, and future studies with greater genome coverage will help to elucidate how plants have managed to adapt to a wide variety of environmental conditions.

  • 45.
    Jansson, Stefan
    et al.
    Umeå University, Faculty of Science and Technology, Department of Plant Physiology. Umeå University, Faculty of Science and Technology, Umeå Plant Science Centre (UPSC).
    Thomas, Howard
    Senescence: developmental program or timetable?2008In: New Phytologist, ISSN 0028-646X, E-ISSN 1469-8137, Vol. 179, no 3, p. 575-579Article in journal (Refereed)
  • 46.
    Johansson, Otilia
    et al.
    Umeå University, Faculty of Science and Technology, Department of Ecology and Environmental Sciences.
    Nordin, Annika
    Olofsson, Johan
    Umeå University, Faculty of Science and Technology, Department of Ecology and Environmental Sciences.
    Palmqvist, Kristin
    Umeå University, Faculty of Science and Technology, Department of Ecology and Environmental Sciences.
    Responses of epiphytic lichens to an experimental whole-tree nitrogen-deposition gradient2010In: New Phytologist, ISSN 0028-646X, E-ISSN 1469-8137, Vol. 188, no 4, p. 1075-1084Article in journal (Refereed)
    Abstract [en]

    • Here, we examined the responses of the epiphytic lichens Alectoria sarmentosa and Platismatia glauca to increased atmospheric nitrogen (N) deposition in an old-growth boreal spruce forest, to assess the sensitivity of these species to N and define their critical N load. • Nitrogen deposition was simulated by irrigating 15 trees over a 3 yr period with water and isotopically labeled NH(4) NO(3) , providing N loads ranging from ambient to 50 kg N ha(-1)  yr(-1) . • Thallus N concentration increased in both species with increasing N load, and uptake rates of both NH(4) (+) and NO(3) (-) were similar. Photobiont concentration increased linearly with increased N in both species, saturating in A. sarmentosa in the third year at the highest N loads (25 and 50 kg ha(-1 ) yr(-1) ). The simulated N deposition decreased the phosphorus (P) concentration in A. sarmentosa, and increased the N : P ratio in both species. • Significant responses in lichen chemistry were detected to inputs of 12.5 kg N ha(-1)  yr(-1) or higher, suggesting that resources other than N limit lichens at higher N loads. However, the data also suggest that N saturation may be cumulative over time, even at low N.

  • 47.
    Johansson, Otilia
    et al.
    Umeå University, Faculty of Science and Technology, Department of Ecology and Environmental Sciences.
    Olofsson, Johan
    Umeå University, Faculty of Science and Technology, Department of Ecology and Environmental Sciences.
    Giesler, Reiner
    Umeå University, Faculty of Science and Technology, Department of Ecology and Environmental Sciences.
    Palmqvist, Kristin
    Umeå University, Faculty of Science and Technology, Department of Ecology and Environmental Sciences.
    Lichen responses to nitrogen and phosphorus additions can be explained by the different symbiont responses2011In: New Phytologist, ISSN 0028-646X, E-ISSN 1469-8137, Vol. 191, no 3, p. 795-805Article in journal (Refereed)
    Abstract [en]

    Responses to simulated nitrogen (N) deposition with or without added phosphorus (P) were investigated for three contrasting lichen species – the N-sensitive Alectoria sarmentosa, the more N-tolerant Platismatia glauca and the N2-fixing Lobaria pulmonaria– in a field experiment.

    To examine whether nutrient limitation differed between the photobiont and the mycobiont within the lichen, the biomass responses of the respective bionts were estimated.

    The lichenized algal cells were generally N-limited, because N-stimulated algal growth in all three species. The mycobiont was P-limited in one species (A. sarmentosa), but the growth response of the mycobionts was complex, as fungal growth is also dependent on a reliable carbon export from the photobiont, which may have been the reason for the decrease of the mycobiont with N addition in P. glauca.

    Our findings showed that P availability was an important factor when studying effects of N deposition, as P supply can both mitigate and intensify the negative effects of N on epiphytic lichens.

  • 48.
    Jokipii-Lukkari, Soile
    et al.
    Umeå University, Faculty of Science and Technology, Umeå Plant Science Centre (UPSC). Umeå University, Faculty of Science and Technology, Department of Plant Physiology. Umeå Plant Science Centre, Department of Forest Genetics and Plant Physiology,Swedish University of Agricultural Sciences, SE-901 84 Umeå, Sweden.
    Sundell, David
    Umeå University, Faculty of Science and Technology, Umeå Plant Science Centre (UPSC). Umeå University, Faculty of Science and Technology, Department of Plant Physiology.
    Nilsson, Ove
    Hvidsten, Torgeir R.
    Umeå University, Faculty of Science and Technology, Umeå Plant Science Centre (UPSC). Umeå University, Faculty of Science and Technology, Department of Plant Physiology. Department of Chemistry, Biotechnology and Food Science, Norwegian University of Life Sciences, 1430 Ås, Norway.
    Street, Nathaniel R.
    Umeå University, Faculty of Science and Technology, Umeå Plant Science Centre (UPSC). Umeå University, Faculty of Science and Technology, Department of Plant Physiology.
    Tuominen, Hannele
    Umeå University, Faculty of Science and Technology, Umeå Plant Science Centre (UPSC). Umeå University, Faculty of Science and Technology, Department of Plant Physiology.
    NorWood: a gene expression resource for evo-devo studies of conifer wood development2017In: New Phytologist, ISSN 0028-646X, E-ISSN 1469-8137, Vol. 216, no 2, p. 482-494Article in journal (Refereed)
    Abstract [en]

    The secondary xylem of conifers is composed mainly of tracheids that differ anatomically and chemically from angiosperm xylem cells. There is currently no high-spatial-resolution data available profiling gene expression during wood formation for any coniferous species, which limits insight into tracheid development.

    RNA-sequencing data from replicated, high-spatial-resolution section series throughout the cambial and woody tissues of Picea abies were used to generate the NorWood.conGenIE.org web resource, which facilitates exploration of the associated gene expression profiles and co-expression networks.

    Integration within PlantGenIE.org enabled a comparative regulomics analysis, revealing divergent co-expression networks between P. abies and the two angiosperm species Arabidopsis thaliana and Populus tremula for the secondary cell wall (SCW) master regulator NAC Class IIB transcription factors. The SCW cellulose synthase genes (CesAs) were located in the neighbourhoods of the NAC factors in Athaliana and P. tremula, but not in Pabies. The NorWood co-expression network enabled identification of potential SCW CesA regulators in P. abies.

    The NorWood web resource represents a powerful community tool for generating evo-devo insights into the divergence of wood formation between angiosperms and gymnosperms and for advancing understanding of the regulation of wood development in P. abies.

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  • 49. Kardol, Paul
    et al.
    De Long, Jonathan R
    Sundqvist, Maja K.
    Crossing the threshold: the power of multi-level experiments in identifying global change responses.2012In: New Phytologist, ISSN 0028-646X, E-ISSN 1469-8137, Vol. 196, no 2, p. 323-6Article in journal (Refereed)
  • 50. Keel, Sonja G.
    et al.
    Campbell, Catherine D.
    Umeå University, Faculty of Science and Technology, Department of Plant Physiology. Umeå University, Faculty of Science and Technology, Umeå Plant Science Centre (UPSC).
    Hogberg, Mona N.
    Richter, Andreas
    Wild, Birgit
    Zhou, Xuhui
    Hurry, Vaughan
    Umeå University, Faculty of Science and Technology, Department of Plant Physiology. Umeå University, Faculty of Science and Technology, Umeå Plant Science Centre (UPSC).
    Linder, Sune
    Nasholm, Torgny
    Hogberg, Peter
    Allocation of carbon to fine root compounds and their residence times in a boreal forest depend on root size class and season2012In: New Phytologist, ISSN 0028-646X, E-ISSN 1469-8137, Vol. 194, no 4, p. 972-981Article in journal (Refereed)
    Abstract [en]

    Fine roots play a key role in the forest carbon balance, but their carbon dynamics remain largely unknown. We pulse labelled 50 m2 patches of young boreal forest by exposure to 13CO2 in early and late summer. Labelled photosynthates were traced into carbon compounds of < 1 and 13 mm diameter roots (fine roots), and into bulk tissue of these and first-order roots (root tips). Root tips were the most strongly labelled size class. Carbon allocation to all size classes was higher in late than in early summer; mean residence times (MRTs) in starch increased from 4 to 11 months. In structural compounds, MRTs were 0.8 yr in tips and 1.8 yr in fine roots. The MRT of carbon in sugars was in the range of days. Functional differences within the fine root population were indicated by carbon allocation patterns and residence times. Pronounced allocation of recent carbon and higher turnover rates in tips are associated with their role in nutrient and water acquisition. In fine roots, longer MRTs but high allocation to sugars and starch reflect their role in structural support and storage. Accounting for heterogeneity in carbon residence times will improve and most probably reduce the estimates of fine root production.

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