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  • 1.
    Ahlström, Anders
    et al.
    Department of Physical Geography and Ecosystem Science, Lund University, Lund, Sweden.
    Canadell, Josep G.
    Global Carbon Project, CSIRO Oceans and Atmosphere, ACT, Canberra, Australia.
    Metcalfe, Daniel B.
    Umeå universitet, Teknisk-naturvetenskapliga fakulteten, Institutionen för ekologi, miljö och geovetenskap.
    Widespread Unquantified Conversion of Old Boreal Forests to Plantations2022Ingår i: Earth's Future, E-ISSN 2328-4277, Vol. 10, nr 11, artikel-id e2022EF003221Artikel i tidskrift (Refereegranskat)
    Abstract [en]

    Across the boreal biome, clear-cutting of old, previously non clear-cut forests with high naturalness followed by tree planting or seeding is a major land use change. However, how much previously uncut forest has been converted to plantations remains unquantified. We combine Swedish national databases on clear-cuts and forest inventories to show that at least 19% of all clear-cuts since 2003 have occurred in old forests that were most likely not previously cut and planted or seeded. Old forests have been cut and lost at a steady rate of ∼1.4% per year for the same period, and at this rate they will disappear by the 2070s. There is further evidence that this type of unreported forest conversion is occurring across much of the world's boreal forest.

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  • 2.
    Avila Clasen, Lina
    et al.
    Department of Biology, University of Copenhagen, Copenhagen, Denmark.
    Permin, Aya
    Department of Biology, University of Copenhagen, Copenhagen, Denmark.
    Horwath, Aline B.
    Biological and Environmental Sciences, Faculty of Natural Sciences, University of Stirling, Stirling, United Kingdom.
    Metcalfe, Daniel B.
    Umeå universitet, Teknisk-naturvetenskapliga fakulteten, Institutionen för ekologi, miljö och geovetenskap. Department of Physical Geography and Ecosystem Science, Lund University, Lund, Sweden.
    Rousk, Kathrin
    Department of Biology, University of Copenhagen, Copenhagen, Denmark.
    Do nitrogen and phosphorus additions affect nitrogen fixation associated with tropical mosses?2023Ingår i: PLANTS, E-ISSN 2223-7747, Vol. 12, nr 7, artikel-id 1443Artikel i tidskrift (Refereegranskat)
    Abstract [en]

    Tropical cloud forests are characterized by abundant and biodiverse mosses which grow epiphytically as well as on the ground. Nitrogen (N)-fixing cyanobacteria live in association with most mosses, and contribute greatly to the N pool via biological nitrogen fixation (BNF). However, the availability of nutrients, especially N and phosphorus (P), can influence BNF rates drastically. To evaluate the effects of increased N and P availability on BNF in mosses, we conducted a laboratory experiment where we added N and P, in isolation and combined, to three mosses (Campylopus sp., Dicranum sp. and Thuidium peruvianum) collected from a cloud forest in Peru. Our results show that N addition almost completely inhibited BNF within a day, whereas P addition caused variable results across moss species. Low N2 fixation rates were observed in Campylopus sp. across the experiment. BNF in Dicranum sp. was decreased by all nutrients, while P additions seemed to promote BNF in T. peruvianum. Hence, each of the three mosses contributes distinctively to the ecosystem N pool depending on nutrient availability. Moreover, increased N input will likely significantly decrease BNF associated with mosses also in tropical cloud forests, thereby limiting N input to these ecosystems via the moss-cyanobacteria pathway.

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  • 3.
    Brum, Mauro
    et al.
    Department of Natural Resources & the Environment, University of New Hampshire, 56 College Rd, Durham, United States.
    Vadeboncoeur, Matthew
    Earth Systems Research Center, University of New Hampshire, 8 College Rd, Durham, United States.
    Asbjornsen, Heidi
    Department of Natural Resources & the Environment, University of New Hampshire, 56 College Rd, Durham, United States; Earth Systems Research Center, University of New Hampshire, 8 College Rd, Durham, United States.
    Puma Vilca, Beisit L.
    Facultad de Ciencias Biológicas, Universidad Nacional de San Antonio Abad del Cusco, Av. de La Cultura 773, Cusco Province 08000, Cusco, Peru; Asociación Civil Sin Fines De Lucro Para La Biodiversidad, Investigación Y Desarrollo Ambiental En Ecosistemas Tropicales (ABIDA), Avenida Argentina F-9, Cusco, Peru.
    Galiano, Darcy
    Facultad de Ciencias Biológicas, Universidad Nacional de San Antonio Abad del Cusco, Av. de La Cultura 773, Cusco Province 08000, Cusco, Peru; Asociación Civil Sin Fines De Lucro Para La Biodiversidad, Investigación Y Desarrollo Ambiental En Ecosistemas Tropicales (ABIDA), Avenida Argentina F-9, Cusco, Peru.
    Horwath, Aline B.
    Asociación Civil Sin Fines De Lucro Para La Biodiversidad, Investigación Y Desarrollo Ambiental En Ecosistemas Tropicales (ABIDA), Avenida Argentina F-9, Cusco, Peru.
    Metcalfe, Daniel B.
    Umeå universitet, Teknisk-naturvetenskapliga fakulteten, Institutionen för ekologi, miljö och geovetenskap.
    Ecophysiological controls on water use of tropical cloud forest trees in response to experimental drought2023Ingår i: Tree Physiology, ISSN 0829-318X, E-ISSN 1758-4469, Vol. 43, nr 9, s. 1514-1532Artikel i tidskrift (Refereegranskat)
    Abstract [en]

    Tropical montane cloud forests (TMCFs) are expected to experience more frequent and prolonged droughts over the coming century, yet understanding of TCMF tree responses to moisture stress remains weak compared with the lowland tropics. We simulated a severe drought in a throughfall reduction experiment (TFR) for 2 years in a Peruvian TCMF and evaluated the physiological responses of several dominant species (Clusia flaviflora Engl., Weinmannia bangii (Rusby) Engl., Weinmannia crassifolia Ruiz & Pav. and Prunus integrifolia (C. Presl) Walp). Measurements were taken of (i) sap flow; (ii) diurnal cycles of stem shrinkage, stem moisture variation and water-use; and (iii) intrinsic water-use efficiency (iWUE) estimated from foliar δ13C. In W. bangii, we used dendrometers and volumetric water content (VWC) sensors to quantify daily cycles of stem water storage. In 2 years of sap flow (Js) data, we found a threshold response of water use to vapor pressure deficit vapor pressure deficit (VPD) > 1.07 kPa independent of treatment, though control trees used more soil water than the treatment trees. The daily decline in water use in the TFR trees was associated with a strong reduction in both morning and afternoon Js rates at a given VPD. Soil moisture also affected the hysteresis strength between Js and VPD. Reduced hysteresis under moisture stress implies that TMCFs are strongly dependent on shallow soil water. Additionally, we suggest that hysteresis can serve as a sensitive indicator of environmental constraints on plant function. Finally, 6 months into the experiment, the TFR treatment significantly increased iWUE in all study species. Our results highlight the conservative behavior of TMCF tree water use under severe soil drought and elucidate physiological thresholds related to VPD and its interaction with soil moisture. The observed strongly isohydric response likely incurs a cost to the carbon balance of the tree and reduces overall ecosystem carbon uptake.

  • 4.
    Cusack, Daniela Francis
    et al.
    Department of Ecosystem Science and Sustainability, Warner College of Natural Resources, Colorado State University, CO, Fort Collins, United States; Smithsonian Tropical Research Institute, Balboa, Panama.
    Addo-Danso, Shalom D.
    CSIR-Forestry Research Institute of Ghana, KNUST, Kumasi, Ghana.
    Agee, Elizabeth A.
    Environmental Sciences Division, Climate Change Sciences Institute, Oak Ridge National Laboratory, TN, Oak Ridge, United States.
    Andersen, Kelly M.
    Asian School of the Environment, Nanyang Technological University, Singapore, Singapore.
    Arnaud, Marie
    IFREMER, Laboratoire Environnement et Ressources des Pertuis Charentais (LER-PC), La Tremblade, France; School of Geography, Earth, and Environmental Sciences, University of Birmingham, Birmingham, United Kingdom.
    Batterman, Sarah A.
    Smithsonian Tropical Research Institute, Balboa, Panama; Cary Institute of Ecosystem Studies, NY, Millbrook, United States; School of Geography, University of Leeds, Leeds, United Kingdom.
    Brearley, Francis Q.
    Department of Natural Sciences, Manchester Metropolitan University, Manchester, United Kingdom.
    Ciochina, Mark I.
    Department of Geography, UCLA, CA, Los Angeles, United States.
    Cordeiro, Amanda L.
    Department of Ecosystem Science and Sustainability, Warner College of Natural Resources, Colorado State University, CO, Fort Collins, United States.
    Dallstream, Caroline
    Department of Biology, Bieler School of Environment, McGill University, QC, Montreal, Canada.
    Diaz-Toribio, Milton H.
    Jardín Botánico Francisco Javier Clavijero, Instituto de Ecología, Xalapa, Mexico.
    Dietterich, Lee H.
    Department of Ecosystem Science and Sustainability, Warner College of Natural Resources, Colorado State University, CO, Fort Collins, United States.
    Fisher, Joshua B.
    Schmid College of Science and Technology, Chapman University, CA, Orange, United States; Joint Institute for Regional Earth System Science and Engineering, University of California, Los Angeles, CA, Los Angeles, United States.
    Fleischer, Katrin
    Department Biogeochemical Signals, Max-Planck-Institute for Biogeochemistry, Jena, Germany.
    Fortunel, Claire
    AMAP (botAnique et Modélisation de l’Architecture des Plantes et des Végétations), Université de Montpellier, CIRAD, CNRS, INRAE, IRD, Montpellier, France.
    Fuchslueger, Lucia
    Centre of Microbiology and Environmental Systems Science, University of Vienna, Vienna, Austria.
    Guerrero-Ramírez, Nathaly R.
    Biodiversity, Macroecology, and Biogeography, Faculty of Forest Sciences and Forest Ecology, University of Göttingen, Göttingen, Germany.
    Kotowska, Martyna M.
    Plant Ecology and Ecosystems Research, Albrecht von Haller Institute for Plant Sciences, University of Göttingen, Göttingen, Germany.
    Lugli, Laynara Figueiredo
    Coordination of Environmental Dynamics, National Institute of Amazonian Research, Manaus, Brazil.
    Marín, César
    Center of Applied Ecology and Sustainability, Pontificia Universidad Católica de Chile, Santiago, Chile; Institute of Botany, The Czech Academy of Sciences, Prùhonice, Czech Republic.
    McCulloch, Lindsay A.
    Department of Ecology and Evolutionary Biology, Brown University, RI, Providence, United States.
    Maeght, Jean-Luc
    AMAP (botAnique et Modélisation de l’Architecture des Plantes et des Végétations), Université de Montpellier, CIRAD, CNRS, INRAE, IRD, Montpellier, France.
    Metcalfe, Daniel B.
    Umeå universitet, Teknisk-naturvetenskapliga fakulteten, Institutionen för ekologi, miljö och geovetenskap.
    Norby, Richard J.
    Department of Ecology and Evolutionary Biology, University of Tennessee, Knoxville, TN, Knoxville, United States.
    Oliveira, Rafael S.
    Department of Plant Biology, Institute of Biology, University of Campinas – UNICAMP, Campinas, Brazil.
    Powers, Jennifer S.
    Department of Plant and Microbial Biology, University of Minnesota, MN, St. Paul, United States; Department of Ecology, Evolution, and Behavior, University of Minnesota, MN, St. Paul, United States.
    Reichert, Tatiana
    School of Life Sciences Weihenstephan, Technical University of Munich, Freising, Germany.
    Smith, Stuart W.
    Asian School of the Environment, Nanyang Technological University, Singapore, Singapore.
    Smith-Martin, Chris M.
    Department of Ecology, Evolution and Environmental Biology, Columbia University, NY, New York, United States.
    Soper, Fiona M.
    Department of Biology, Bieler School of Environment, McGill University, QC, Montreal, Canada.
    Toro, Laura
    Department of Plant and Microbial Biology, University of Minnesota, MN, St. Paul, United States; Department of Ecology, Evolution, and Behavior, University of Minnesota, MN, St. Paul, United States.
    Umaña, Maria N.
    Department of Ecology and Evolutionary Biology, University of Michigan, MI, Ann Arbor, United States.
    Valverde-Barrantes, Oscar
    Department of Biological Sciences, Institute of Environment, International Center of Tropical Biodiversity, Florida International University, FL, Miami, United States.
    Weemstra, Monique
    Department of Ecology and Evolutionary Biology, University of Michigan, MI, Ann Arbor, United States.
    Werden, Leland K.
    Lyon Arboretum, University of Hawaii at Mânoa, HI, Honolulu, United States.
    Wong, Michelle
    Cary Institute of Ecosystem Studies, NY, Millbrook, United States.
    Wright, Cynthia L.
    Environmental Sciences Division, Climate Change Sciences Institute, Oak Ridge National Laboratory, TN, Oak Ridge, United States.
    Wright, Stuart Joseph
    Smithsonian Tropical Research Institute, Balboa, Panama.
    Yaffar, Daniela
    Environmental Sciences Division, Climate Change Sciences Institute, Oak Ridge National Laboratory, TN, Oak Ridge, United States; Department of Ecology and Evolutionary Biology, University of Tennessee, Knoxville, TN, Knoxville, United States.
    Tradeoffs and Synergies in Tropical Forest Root Traits and Dynamics for Nutrient and Water Acquisition: Field and Modeling Advances2021Ingår i: Frontiers in Forests and Global Change, E-ISSN 2624-893X, Vol. 4, artikel-id 704469Artikel, forskningsöversikt (Refereegranskat)
    Abstract [en]

    Vegetation processes are fundamentally limited by nutrient and water availability, the uptake of which is mediated by plant roots in terrestrial ecosystems. While tropical forests play a central role in global water, carbon, and nutrient cycling, we know very little about tradeoffs and synergies in root traits that respond to resource scarcity. Tropical trees face a unique set of resource limitations, with rock-derived nutrients and moisture seasonality governing many ecosystem functions, and nutrient versus water availability often separated spatially and temporally. Root traits that characterize biomass, depth distributions, production and phenology, morphology, physiology, chemistry, and symbiotic relationships can be predictive of plants’ capacities to access and acquire nutrients and water, with links to aboveground processes like transpiration, wood productivity, and leaf phenology. In this review, we identify an emerging trend in the literature that tropical fine root biomass and production in surface soils are greatest in infertile or sufficiently moist soils. We also identify interesting paradoxes in tropical forest root responses to changing resources that merit further exploration. For example, specific root length, which typically increases under resource scarcity to expand the volume of soil explored, instead can increase with greater base cation availability, both across natural tropical forest gradients and in fertilization experiments. Also, nutrient additions, rather than reducing mycorrhizal colonization of fine roots as might be expected, increased colonization rates under scenarios of water scarcity in some forests. Efforts to include fine root traits and functions in vegetation models have grown more sophisticated over time, yet there is a disconnect between the emphasis in models characterizing nutrient and water uptake rates and carbon costs versus the emphasis in field experiments on measuring root biomass, production, and morphology in response to changes in resource availability. Closer integration of field and modeling efforts could connect mechanistic investigation of fine-root dynamics to ecosystem-scale understanding of nutrient and water cycling, allowing us to better predict tropical forest-climate feedbacks.

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  • 5.
    Eckdahl, Johan A.
    et al.
    Umeå universitet, Teknisk-naturvetenskapliga fakulteten, Institutionen för ekologi, miljö och geovetenskap. Department of Physical Geography and Ecosystem Science, Lund University, Lund, Sweden.
    Kristensen, Jeppe A.
    Metcalfe, Daniel B.
    Umeå universitet, Teknisk-naturvetenskapliga fakulteten, Institutionen för ekologi, miljö och geovetenskap.
    Climate and forest properties explain wildfire impact on microbial community and nutrient mobilization in boreal soil2023Ingår i: Frontiers in Forests and Global Change, E-ISSN 2624-893X, Vol. 6, artikel-id 1136354Artikel i tidskrift (Refereegranskat)
    Abstract [en]

    The boreal landscape stores an estimated 40% of the earth's carbon (C) found in terrestrial vegetation and soils, with a large portion collected in thick organic soil layers. These ground stores are subject to substantial removals due to the centurial return of wildfire, which has strong impacts on the soil microbial community and nutrient cycling, which in turn can control ecosystem recovery patterns and process rates, such as C turnover. Currently, predictive knowledge used in assessing fire impacts is largely focused on ecosystems that experience only superficial burning and few robust observations exist regarding the effect that smoldering combustion in deeper active soil layers has on post-fire soil activity. This study provided a highly replicated and regionally extensive survey of wildfire impact on microbial community structure (using fatty acid biomarkers) and nutrient cycling (using in situ ionic resin capsules) across broad gradients of climate, forest properties and fire conditions within 50 separate burn scars and 50 additional matched unburnt boreal forest soils. The results suggest a strong metabolic shift in burnt soils due to heat impact on their structure and a decoupling from aboveground processes, releasing ecosystem N limitation and increasing mobilization of N, P, K, and S as excess in conjunction with an altered, C-starved microbial community structure and reduced root uptake due to vegetation mortality. An additional observed climatic control over burnt soil properties has implications for altered boreal forest function in future climate and fire regimes deserving of further attention.

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  • 6.
    Eckdahl, Johan A.
    et al.
    Umeå universitet, Teknisk-naturvetenskapliga fakulteten, Institutionen för ekologi, miljö och geovetenskap. Department Of Physical Geography And Ecosystem Science, Lund University, Lund, Sweden.
    Kristensen, Jeppe A.
    Environmental Change Institute, School Of Geography And The Environment, University Of Oxford, Oxford, United Kingdom.
    Metcalfe, Daniel B.
    Umeå universitet, Teknisk-naturvetenskapliga fakulteten, Institutionen för ekologi, miljö och geovetenskap.
    Climatic variation drives loss and restructuring of carbon and nitrogen in boreal forest wildfire2022Ingår i: Biogeosciences, ISSN 1726-4170, E-ISSN 1726-4189, Vol. 19, nr 9, s. 2487-2506Artikel i tidskrift (Refereegranskat)
    Abstract [en]

    The boreal forest landscape covers approximately 10% of the earth's land area and accounts for almost 30 % of the global annual terrestrial sink of carbon (C). Increased emissions due to climate-change-amplified fire frequency, size, and intensity threaten to remove elements such as C and nitrogen (N) from forest soil and vegetation at rates faster than they accumulate. This may result in large areas within the region becoming a net source of greenhouse gases, creating a positive feedback loop with a changing climate. Meter-scale estimates of area-normalized fire emissions are limited in Eurasian boreal forests, and knowledge of their relation to climate and ecosystem properties is sparse. This study sampled 50 separate Swedish wildfires, which occurred during an extreme fire season in 2018, providing quantitative estimates of C and N loss due to fire along a climate gradient. Mean annual precipitation had strong positive effects on total fuel, which was the strongest driver for increasing C and N losses. Mean annual temperature (MAT) influenced both pre-and postfire organic layer soil bulk density and C: N ratio, which had mixed effects on C and N losses. Significant fire-induced loss of C estimated in the 50 plots was comparable to estimates in similar Eurasian forests but approximately a quarter of those found in typically more intense North American boreal wildfires. N loss was insignificant, though a large amount of fire-affected fuel was converted to a low C: N surface layer of char in proportion to increased MAT. These results reveal large quantitative differences in C and N losses between global regions and their linkage to the broad range of climate conditions within Fennoscandia. A need exists to better incorporate these factors into models to improve estimates of global emissions of C and N due to fire in future climate scenarios. Additionally, this study demonstrated a linkage between climate and the extent of charring of soil fuel and discusses its potential for altering C and N dynamics in postfire recovery.

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  • 7.
    Eckdahl, Johan A.
    et al.
    Umeå universitet, Teknisk-naturvetenskapliga fakulteten, Institutionen för ekologi, miljö och geovetenskap. Department of Physical Geography and Ecosystem Science, Lund University, Lund, Sweden.
    Kristensen, Jeppe A.
    Environmental Change Institute, School of Geography and the Environment, University of Oxford, Oxford, United Kingdom; Department of Biology, Aarhus University, Aarhus, Denmark.
    Metcalfe, Daniel B.
    Umeå universitet, Teknisk-naturvetenskapliga fakulteten, Institutionen för ekologi, miljö och geovetenskap.
    Restricted plant diversity limits carbon recapture after wildfire in warming boreal forests2024Ingår i: Communications Earth & Environment, E-ISSN 2662-4435, Vol. 5, nr 1, artikel-id 186Artikel i tidskrift (Refereegranskat)
    Abstract [en]

    Incomplete wildfire combustion in boreal forests leaves behind legacy plant-soil feedbacks known to restrict plant biodiversity. These restrictions can inhibit carbon recapture after fire by limiting ecosystem transition to vegetation growth patterns that are capable of offsetting warmth-enhanced soil decomposition under climate change. Here, we field-surveyed plant regrowth conditions 2 years after 49 separate, naturally-occurring wildfires spanning the near-entire climatic range of boreal Fennoscandia in order to determine the local to regional scale drivers of early vegetation recovery. Minimal conifer reestablishment was found across a broad range of fire severities, though residual organic soil and plant structure was associated with restricted growth of a variety of more warmth-adapted vegetation, such as broadleaf trees. This dual regeneration limitation coincided with greater concentrations of bacterial decomposers in the soil under increased mean annual temperature, potentially enhancing soil carbon release. These results suggest that large portions of the boreal region are currently at risk of extending postfire periods of net emissions of carbon to the atmosphere under limitations in plant biodiversity generated by wildfire and a changing climate.

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  • 8.
    Eckdahl, Johan A.
    et al.
    Umeå universitet, Teknisk-naturvetenskapliga fakulteten, Institutionen för ekologi, miljö och geovetenskap. Department of Physical Geography and Ecosystem Science, Lund University, Lund, Sweden.
    Rodriguez, Pere Casal
    Department of Geology, Lund University, Lund, Sweden.
    Kristensen, Jeppe A.
    Environmental Change Institute, School of Geography and the Environment, University of Oxford, Oxford, United Kingdom.
    Metcalfe, Daniel B.
    Umeå universitet, Teknisk-naturvetenskapliga fakulteten, Institutionen för ekologi, miljö och geovetenskap.
    Ljung, Karl
    Department of Geology, Lund University, Lund, Sweden.
    Mineral soils are an important intermediate storage pool of black carbon in fennoscandian boreal forests2022Ingår i: Global Biogeochemical Cycles, ISSN 0886-6236, E-ISSN 1944-9224, Vol. 36, nr 11, artikel-id e2022GB007489Artikel i tidskrift (Refereegranskat)
    Abstract [en]

    Approximately 40% of earth's carbon (C) stored in land vegetation and soil is within the boreal region. This large C pool is subjected to substantial removals and transformations during periodic wildfire. Fire-altered C, commonly known as pyrogenic carbon (PyC), plays a significant role in forest ecosystem functioning and composes a considerable fraction of C transport to limnic and oceanic sediments. While PyC stores are beginning to be quantified globally, knowledge is lacking regarding the drivers of their production and transport across ecosystems. This study used the chemo-thermal oxidation at 375°C (CTO-375) method to isolate a particularly refractory subset of PyC compounds, here called black carbon (BC), finding an average increase of 11.6 g BC m−2 at 1 year postfire in 50 separate wildfires occurring in Sweden during 2018. These increases could not be linked to proposed drivers, however BC storage in 50 additional nearby unburnt soils related strongly to soil mass while its proportion of the larger C pool related negatively to soil C:N. Fire approximately doubled BC stocks in the mineral layer but had no significant effect on BC in the organic layer where it was likely produced. Suppressed decomposition rates and low heating during fire in mineral subsoil relative to upper layers suggests potential removals of the doubled mineral layer BC are more likely transported out of the soil system than degraded in situ. Therefore, mineral soils are suggested to be an important storage pool for BC that can buffer short-term (production in fire) and long-term (cross-ecosystem transport) BC cycling.

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  • 9.
    Gundale, Michael J.
    et al.
    Department of Forest Ecology and Management, Swedish University of Agricultural Sciences, Umeå, Sweden.
    Axelsson, E. Petter
    Department of Wildlife, Fish and Environmental Studies, Swedish University of Agricultural Sciences, Umeå, Sweden.
    Buness, Vincent
    Department of Forest Ecology and Management, Swedish University of Agricultural Sciences, Umeå, Sweden.
    Callebaut, Timon
    Umeå universitet, Teknisk-naturvetenskapliga fakulteten, Institutionen för ekologi, miljö och geovetenskap.
    DeLuca, Thomas H.
    College of Forestry, Oregon State University, OR, Corvallis, United States.
    Hupperts, Stefan F.
    Department of Forest Ecology and Management, Swedish University of Agricultural Sciences, Umeå, Sweden.
    Ibáñez, Theresa S.
    Department of Wildlife, Fish and Environmental Studies, Swedish University of Agricultural Sciences, Umeå, Sweden.
    Metcalfe, Daniel B.
    Umeå universitet, Teknisk-naturvetenskapliga fakulteten, Institutionen för ekologi, miljö och geovetenskap.
    Nilsson, Marie-Charlotte
    Department of Forest Ecology and Management, Swedish University of Agricultural Sciences, Umeå, Sweden.
    Peichl, Matthias
    Department of Forest Ecology and Management, Swedish University of Agricultural Sciences, Umeå, Sweden.
    Spitzer, Clydecia M.
    Department of Forest Ecology and Management, Swedish University of Agricultural Sciences, Umeå, Sweden.
    Stangl, Zsofia R.
    Department of Forest Ecology and Management, Swedish University of Agricultural Sciences, Umeå, Sweden.
    Strengbom, Joachim
    Department of Ecology, Swedish University of Agricultural Sciences, Uppsala, Sweden.
    Sundqvist, Maja K.
    Department of Forest Ecology and Management, Swedish University of Agricultural Sciences, Umeå, Sweden.
    Wardle, David A.
    Umeå universitet, Teknisk-naturvetenskapliga fakulteten, Institutionen för ekologi, miljö och geovetenskap.
    Lindahl, Björn D.
    Department of Soil Science, Swedish University of Agricultural Sciences, Uppsala, Sweden.
    The biological controls of soil carbon accumulation following wildfire and harvest in boreal forests: a review2024Ingår i: Global Change Biology, ISSN 1354-1013, E-ISSN 1365-2486, Vol. 30, nr 5, artikel-id e17276Artikel, forskningsöversikt (Refereegranskat)
    Abstract [en]

    Boreal forests are frequently subjected to disturbances, including wildfire and clear-cutting. While these disturbances can cause soil carbon (C) losses, the long-term accumulation dynamics of soil C stocks during subsequent stand development is controlled by biological processes related to the balance of net primary production (NPP) and outputs via heterotrophic respiration and leaching, many of which remain poorly understood. We review the biological processes suggested to influence soil C accumulation in boreal forests. Our review indicates that median C accumulation rates following wildfire and clear-cutting are similar (0.15 and 0.20 Mg ha−1 year−1, respectively), however, variation between studies is extremely high. Further, while many individual studies show linear increases in soil C stocks through time after disturbance, there are indications that C stock recovery is fastest early to mid-succession (e.g. 15–80 years) and then slows as forests mature (e.g. >100 years). We indicate that the rapid build-up of soil C in younger stands appears not only driven by higher plant production, but also by a high rate of mycorrhizal hyphal production, and mycorrhizal suppression of saprotrophs. As stands mature, the balance between reductions in plant and mycorrhizal production, increasing plant litter recalcitrance, and ectomycorrhizal decomposers and saprotrophs have been highlighted as key controls on soil C accumulation rates. While some of these controls appear well understood (e.g. temporal patterns in NPP, changes in aboveground litter quality), many others remain research frontiers. Notably, very little data exists describing and comparing successional patterns of root production, mycorrhizal functional traits, mycorrhizal-saprotroph interactions, or C outputs via heterotrophic respiration and dissolved organic C following different disturbances. We argue that these less frequently described controls require attention, as they will be key not only for understanding ecosystem C balances, but also for representing these dynamics more accurately in soil organic C and Earth system models.

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  • 10.
    Gärtner, Antje
    et al.
    Department of Physical Geography and Ecosystem Science, Lund University, Lund, Sweden.
    Jönsson, Anna Maria
    Department of Physical Geography and Ecosystem Science, Lund University, Lund, Sweden.
    Metcalfe, Daniel B.
    Umeå universitet, Teknisk-naturvetenskapliga fakulteten, Institutionen för ekologi, miljö och geovetenskap. Department of Physical Geography and Ecosystem Science, Lund University, Lund, Sweden.
    Pugh, Thomas A. M.
    Department of Physical Geography and Ecosystem Science, Lund University, Lund, Sweden; School of Geography, Earth & Environmental Sciences, University of Birmingham, Birmingham, United Kingdom; Birmingham Institute of Forest Research, University of Birmingham, Birmingham, United Kingdom.
    Tagesson, Torbern
    Department of Physical Geography and Ecosystem Science, Lund University, Lund, Sweden; Department of Geosciences and Natural Resource Management, University of Copenhagen, Copenhagen, Denmark.
    Ahlström, Anders
    Department of Physical Geography and Ecosystem Science, Lund University, Lund, Sweden.
    Temperature and tree size explain the mean time to fall of dead standing trees across large scales2023Ingår i: Forests, E-ISSN 1999-4907, Vol. 14, nr 5, artikel-id 1017Artikel i tidskrift (Refereegranskat)
    Abstract [en]

    Dead standing trees (DSTs) generally decompose slower than wood in contact with the forest floor. In many regions, DSTs are being created at an increasing rate due to accelerating tree mortality caused by climate change. Therefore, factors determining DST fall are crucial for predicting dead wood turnover time but remain poorly constrained. Here, we conduct a re-analysis of published DST fall data to provide standardized information on the mean time to fall (MTF) of DSTs across biomes. We used multiple linear regression to test covariates considered important for DST fall, while controlling for mortality and management effects. DSTs of species killed by fire, insects and other causes stood on average for 48, 13 and 19 years, but MTF calculations were sensitive to how tree size was accounted for. Species’ MTFs differed significantly between DSTs killed by fire and other causes, between coniferous and broadleaved plant functional types (PFTs) and between managed and unmanaged sites, but management did not explain MTFs when we distinguished by mortality cause. Mean annual temperature (MAT) negatively affected MTFs, whereas larger tree size or being coniferous caused DSTs to stand longer. The most important explanatory variables were MAT and tree size, with minor contributions of management and plant functional type depending on mortality cause. Our results provide a basis to improve the representation of dead wood decomposition in carbon cycle assessments.

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  • 11.
    Huaraca Huasco, Walter
    et al.
    Environmental Change Institute, School of Geography and the Environment, University of Oxford, Oxford, United Kingdom.
    Riutta, Terhi
    Environmental Change Institute, School of Geography and the Environment, University of Oxford, Oxford, United Kingdom.
    Girardin, Cécile A. J.
    Environmental Change Institute, School of Geography and the Environment, University of Oxford, Oxford, United Kingdom.
    Hancco Pacha, Fernando
    Universidad Nacional de San Antonio Abad del Cusco, Cusco, Peru.
    Puma Vilca, Beisit L.
    Universidad Nacional de San Antonio Abad del Cusco, Cusco, Peru.
    Moore, Sam
    Environmental Change Institute, School of Geography and the Environment, University of Oxford, Oxford, United Kingdom.
    Rifai, Sami W.
    ARC Centre of Excellence for Climate Extremes, University of New South Wales, NSW, Sydney, Australia.
    del Aguila-Pasquel, Jhon
    Instituto de Investigaciones de la Amazonía Peruana (IIAP), Iquitos, Peru.
    Araujo Murakami, Alejandro
    Museo de Historia Natural Noel Kempff Mercado Universidad Autónoma Gabriel Rene Moreno, Santa Cruz, Bolivia.
    Freitag, Renata
    Programa de Pós-graduação em Ecologia e Conservação, Universidade do Estado de Mato Grosso, MT, Nova Xavantina, Brazil.
    Morel, Alexandra C.
    Department of Geography and Environmental Science, University of Dundee, Dundee, United Kingdom.
    Demissie, Sheleme
    Environment and Coffee Forest Forum, Addis Ababa, Ethiopia.
    Doughty, Christopher E.
    School of Informatics, Computing and Cyber systems, Northern Arizona University, AZ, Flagstaff, United States.
    Oliveras, Imma
    Environmental Change Institute, School of Geography and the Environment, University of Oxford, Oxford, United Kingdom.
    Galiano Cabrera, Darcy F.
    Universidad Nacional de San Antonio Abad del Cusco, Cusco, Peru.
    Durand Baca, Liliana
    Universidad Nacional Federico Villarreal de Lima, Lima, Peru.
    Farfán Amézquita, Filio
    Universidad Nacional de San Antonio Abad del Cusco, Cusco, Peru.
    Silva Espejo, Javier E.
    Departamento de Biología, Universidad de La Serena, La Serena, Chile.
    da Costa, Antonio C.L.
    Instituto de Geosciências, Universidade Federal do Pará, Belém, Brazil.
    Oblitas Mendoza, Erick
    Instituto Nacional de Pesquisas da Amazônia, Manaus, Brazil.
    Quesada, Carlos Alberto
    Instituto Nacional de Pesquisas da Amazônia, Manaus, Brazil.
    Evouna Ondo, Fidele
    Agence Nationale des Parcs Nationaux, Libreville, Gabon.
    Edzang Ndong, Josué
    Agence Nationale des Parcs Nationaux, Libreville, Gabon.
    Jeffery, Kathryn J.
    Faculty of Natural Sciences, University of Stirling, Stirling, United Kingdom.
    Mihindou, Vianet
    Ministère de la Foret, de la Mer, de l'Environnement, Chargé Du Plan Climat, Libreville, Gabon.
    White, Lee J. T.
    Ministère de la Foret, de la Mer, de l'Environnement, Chargé Du Plan Climat, Libreville, Gabon.
    N'ssi Bengone, Natacha
    Ministère de la Foret, de la Mer, de l'Environnement, Chargé Du Plan Climat, Libreville, Gabon.
    Ibrahim, Forzia
    Forestry Research Institute of Ghana, Council for Scientific and Industrial Research, University, Kumasi, Ghana.
    Addo-Danso, Shalom D.
    Forestry Research Institute of Ghana, Council for Scientific and Industrial Research, University, Kumasi, Ghana.
    Duah-Gyamfi, Akwasi
    Forestry Research Institute of Ghana, Council for Scientific and Industrial Research, University, Kumasi, Ghana.
    Djaney Djagbletey, Gloria
    Forestry Research Institute of Ghana, Council for Scientific and Industrial Research, University, Kumasi, Ghana.
    Owusu-Afriyie, Kennedy
    Forestry Research Institute of Ghana, Council for Scientific and Industrial Research, University, Kumasi, Ghana.
    Amissah, Lucy
    Forestry Research Institute of Ghana, Council for Scientific and Industrial Research, University, Kumasi, Ghana.
    Mbou, Armel T.
    Centro Euro-Mediterraneo sui Cambiamenti Climatici, Leece, Italy.
    Marthews, Toby R.
    UK Centre for Ecology & Hydrology (UKCEH), Wallingford, United Kingdom.
    Metcalfe, Daniel B.
    Umeå universitet, Teknisk-naturvetenskapliga fakulteten, Institutionen för ekologi, miljö och geovetenskap.
    Aragão, Luiz E. O.
    Divisão de Sensoriamento Remoto-DIDSR, Instituto Nacional de Pesquisas Espaciais, SP, São Jose dos Campos, Brazil.
    Marimon-Junior, Ben H.
    Programa de Pós-graduação em Ecologia e Conservação, Universidade do Estado de Mato Grosso, MT, Nova Xavantina, Brazil.
    Marimon, Beatriz S.
    Programa de Pós-graduação em Ecologia e Conservação, Universidade do Estado de Mato Grosso, MT, Nova Xavantina, Brazil.
    Majalap, Noreen
    Sabah Forestry Department, Forest Research Centre, Sabah, Malaysia.
    Adu-Bredu, Stephen
    Forestry Research Institute of Ghana, Council for Scientific and Industrial Research, University, Kumasi, Ghana.
    Abernethy, Katharine A.
    Faculty of Natural Sciences, University of Stirling, Stirling, United Kingdom.
    Silman, Miles
    Department of Biology, Wake Forest University, NC, Winston-Salem, United States.
    Ewers, Robert M.
    Department of Life Science, Imperial College London, Ascot, United Kingdom.
    Meir, Patrick
    Research School of Biology, Australian National University, ACT, Canberra, Australia; School of Geosciences, University of Edinburgh, Edinburgh, United Kingdom.
    Malhi, Yadvinder
    Environmental Change Institute, School of Geography and the Environment, University of Oxford, Oxford, United Kingdom.
    Fine root dynamics across pantropical rainforest ecosystems2021Ingår i: Global Change Biology, ISSN 1354-1013, E-ISSN 1365-2486, Vol. 27, nr 15, s. 3657-3680Artikel i tidskrift (Refereegranskat)
    Abstract [en]

    Fine roots constitute a significant component of the net primary productivity (NPP) of forest ecosystems but are much less studied than aboveground NPP. Comparisons across sites and regions are also hampered by inconsistent methodologies, especially in tropical areas. Here, we present a novel dataset of fine root biomass, productivity, residence time, and allocation in tropical old-growth rainforest sites worldwide, measured using consistent methods, and examine how these variables are related to consistently determined soil and climatic characteristics. Our pantropical dataset spans intensive monitoring plots in lowland (wet, semi-deciduous, and deciduous) and montane tropical forests in South America, Africa, and Southeast Asia (n = 47). Large spatial variation in fine root dynamics was observed across montane and lowland forest types. In lowland forests, we found a strong positive linear relationship between fine root productivity and sand content, this relationship was even stronger when we considered the fractional allocation of total NPP to fine roots, demonstrating that understanding allocation adds explanatory power to understanding fine root productivity and total NPP. Fine root residence time was a function of multiple factors: soil sand content, soil pH, and maximum water deficit, with longest residence times in acidic, sandy, and water-stressed soils. In tropical montane forests, on the other hand, a different set of relationships prevailed, highlighting the very different nature of montane and lowland forest biomes. Root productivity was a strong positive linear function of mean annual temperature, root residence time was a strong positive function of soil nitrogen content in montane forests, and lastly decreasing soil P content increased allocation of productivity to fine roots. In contrast to the lowlands, environmental conditions were a better predictor for fine root productivity than for fractional allocation of total NPP to fine roots, suggesting that root productivity is a particularly strong driver of NPP allocation in tropical mountain regions.

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  • 12.
    Hwang, Bernice C.
    et al.
    Department of Physical Geography and Ecosystem Science, Lund University, Lund, Sweden.
    Giardina, Christian P.
    Pacific Southwest Research Station, USDA Forest Service, Institute of Pacific Islands Forestry, HI, Hilo, United States.
    Litton, Creighton M.
    Department of Natural Resources and Environmental Management, University of Hawai‘i at Mānoa, HI, Honolulu, United States.
    Francisco, Kainana S.
    Pacific Southwest Research Station, USDA Forest Service, Institute of Pacific Islands Forestry, HI, Hilo, United States.
    Pacheco, Cody
    Pacific Southwest Research Station, USDA Forest Service, Institute of Pacific Islands Forestry, HI, Hilo, United States.
    Thomas, Naneaikealaula
    Pacific Southwest Research Station, USDA Forest Service, Institute of Pacific Islands Forestry, HI, Hilo, United States.
    Uehara, Tyler
    Pacific Southwest Research Station, USDA Forest Service, Institute of Pacific Islands Forestry, HI, Hilo, United States.
    Metcalfe, Daniel B.
    Umeå universitet, Teknisk-naturvetenskapliga fakulteten, Institutionen för ekologi, miljö och geovetenskap. Department of Physical Geography and Ecosystem Science, Lund University, Lund, Sweden.
    Impacts of insect frass and cadavers on soil surface litter decomposition along a tropical forest temperature gradient2022Ingår i: Ecology and Evolution, E-ISSN 2045-7758, Vol. 12, nr 9, artikel-id e9322Artikel i tidskrift (Refereegranskat)
    Abstract [en]

    Insect herbivores play important roles in shaping many ecosystem processes, but how climate change will alter the effects of insect herbivory are poorly understood. To address this knowledge gap, we quantified for the first time how insect frass and cadavers affected leaf litter decomposition rates and nutrient release along a highly constrained 4.3°C mean annual temperature (MAT) gradient in a Hawaiian montane tropical wet forest. We constructed litterbags of standardized locally sourced leaf litter, with some amended with insect frass + cadavers to produce treatments designed to simulate ambient (Control = no amendment), moderate (Amended-Low = 2 × Control level), or severe (Amended-High = 11 × Control level) insect outbreak events. Multiple sets of these litterbags were deployed across the MAT gradient, with individual litterbags collected periodically over one year to assess how rising MAT altered the effects of insect deposits on litter decomposition rates and nitrogen (N) release. Increased MAT and insect inputs additively increased litter decomposition rates and N immobilization rates, with effects being stronger for Amended-High litterbags. However, the apparent temperature sensitivity (Q10) of litter decomposition was not clearly affected by amendments. The effects of adding insect deposits in this study operated differently than the slower litter decomposition and greater N mobilization rates often observed in experiments which use chemical fertilizers (e.g., urea, ammonium nitrate). Further research is required to understand mechanistic differences between amendment types. Potential increases in outbreak-related herbivore deposits coupled with climate warming will accelerate litter decomposition and nutrient cycling rates with short-term consequences for nutrient cycling and carbon storage in tropical montane wet forests.

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  • 13.
    Hwang, Bernice C.
    et al.
    Department of Physical Geography and Ecosystem Science, Lund University, Lund, Sweden.
    Metcalfe, Daniel B.
    Umeå universitet, Teknisk-naturvetenskapliga fakulteten, Institutionen för ekologi, miljö och geovetenskap. Department of Physical Geography and Ecosystem Science, Lund University, Lund, Sweden.
    Reviews and syntheses: Impacts of plant-silica-herbivore interactions on terrestrial biogeochemical cycling2021Ingår i: Biogeosciences, ISSN 1726-4170, E-ISSN 1726-4189, Vol. 18, nr 4, s. 1259-1268Artikel, forskningsöversikt (Refereegranskat)
    Abstract [en]

    Researchers have known for decades that silicon plays a major role in biogeochemical and plant-soil processes in terrestrial systems. Meanwhile, plant biologists continue to uncover a growing list of benefits derived from silicon to combat abiotic and biotic stresses, such as defense against herbivory. Yet despite growing recognition of herbivores as important ecosystem engineers, many major gaps remain in our understanding of how silicon and herbivory interact to shape biogeochemical processes, particularly in natural systems. We review and synthesize 119 available studies directly investigating silicon and herbivory to summarize key trends and highlight research gaps and opportunities. Categorizing studies by multiple ecosystem, plant, and herbivore characteristics, we find substantial evidence for a wide variety of important interactions between plant silicon and herbivory but highlight the need for more research particularly in non-graminoid-dominated vegetation outside of the temperate biome as well as on the potential effects of herbivory on silicon cycling. Continuing to overlook silicon-herbivory dynamics in natural ecosystems limits our understanding of potentially critical animal-plant-soil feedbacks necessary to inform land management decisions and to refine global models of environmental change.

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  • 14.
    Hwang, Bernice
    et al.
    Umeå universitet, Teknisk-naturvetenskapliga fakulteten, Institutionen för ekologi, miljö och geovetenskap. Department of Physical Geography and Ecosystem Science, Lund University, Lund, Sweden; Department of Ecology, University of Innsbruck, Sterwartestraße 15, Innsbruck, Austria.
    Giardina, Christian P.
    Institute of Pacific Islands Forestry, Pacific Southwest Research Station, USDA Forest Service, HI, Hilo, United States.
    Adu-Bredu, Stephen
    CSIR-Forestry Research Institute of Ghana: Kumasi, Ashanti, Ghana; Department of Natural Resources Management, CSIR College of Science and Technology, Kumasi, Ghana.
    Barrios-Garcia, M. Noelia
    Rubenstein School of Environment and Natural Resources, University of Vermont, VT, Burlington, United States; CONICET, CENAC-APN, Universidad Nacional del Comahue (CRUB), Bariloche, Argentina.
    Calvo-Alvarado, Julio C.
    Escuela de Ingeniería Forestal, Tecnológico de Costa Rica, Cartago, Costa Rica.
    Dargie, Greta C.
    School of Geography, University of Leeds, Leeds, United Kingdom.
    Diao, Haoyu
    CAS Key Laboratory of Forest Ecology and Management, Institute of Applied Ecology, Chinese Academy of Sciences, Shenyang, China; Swiss Federal Institute for Forest, Snow and Landscape Research WSL, Birmensdorf, Switzerland.
    Duboscq-Carra, Virginia G.
    Grupo de Ecología de Invasiones, Instituto de Investigaciones en Biodiversidad y Medioambiente (INIBIOMA)—CONICET—Universidad Nacional del Comahue, Bariloche, Argentina.
    Hemp, Andreas
    Department of Plant Systematics, University of Bayreuth, Bayreuth, Germany.
    Hemp, Claudia
    Department of Plant Systematics, University of Bayreuth, Bayreuth, Germany; Senckenberg Biodiversity and Climate Research Centre, Frankfurt, Germany.
    Huasco, Walter Huaraca
    Environmental Change Institute, School of Geography and the Environment, University of Oxford, Oxford, United Kingdom; Asociación Civil Sin Fines De Lucro Para La Biodiversidad, Investigación Y Desarrollo Ambiental En Ecosistemas Tropicales (ABIDA), Urbanización Ucchullo Grande, Avenida Argentina F-9, Cusco, Peru.
    Ivanov, Aleksandr V.
    Institute of Geology and Nature Management Far Eastern Branch of Russian Academy of Sciences, Relochny lane, 1, Blagoveshchensk, Russian Federation.
    Johnson, Nels G.
    Pacific Southwest Research Station, USDA Forest Service, HI, Hilo, United States.
    Kuijper, Dries P. J.
    Mammal Research Institute, Polish Academy of Sciences, Ul. Stoczek 1, Białowieża, Poland.
    Lewis, Simon L.
    School of Geography, University of Leeds, Leeds, United Kingdom; Department of Geography, University College London, London, United Kingdom.
    Lobos-Catalán, Paulina
    Instituto de Ciencias Ambientales y Evolutivas, Universidad Austral de Chile, Campus Isla Teja, Valdivia, Chile.
    Malhi, Yadvinder
    Environmental Change Institute, School of Geography and the Environment, University of Oxford, Oxford, United Kingdom.
    Marshall, Andrew R.
    Forest Research Institute, University of the Sunshine Coast, Sippy Downs, QLD, Australia; Reforest Africa, PO Box 5, Kilombero District, Mang’ula, Tanzania.
    Mumladze, Levan
    Institute of Zoology, Ilia State University, 3/5 Cholokashvili Ave, Tbilisi, Georgia.
    Ngute, Alain Senghor K.
    Forest Research Institute, University of the Sunshine Coast, Sippy Downs, QLD, Australia.
    Palma, Ana C.
    College of Science & amp; Engineering and Centre for Tropical Environmental and Sustainability Science, James Cook University, QLD, Australia.
    Petritan, Ion Catalin
    Faculty of Silviculture and Forest Engineering, Transilvania University of Brașov, Șirul Beethoven 1, Brașov, Romania.
    Rordriguez-Cabal, Mariano A.
    Rubenstein School of Environment and Natural Resources, University of Vermont, VT, Burlington, United States; Grupo de Ecología de Invasiones, Instituto de Investigaciones en Biodiversidad y Medioambiente (INIBIOMA)—CONICET—Universidad Nacional del Comahue, Bariloche, Argentina.
    Suspense, Ifo A.
    Ecole Nationale Supérieure d’Agronomie et de Foresterie, Université Marien Ngouabi, Brazzaville, Congo; Laboratoire de Biodiversité, de Gestion des Ecosystèmes et de l’Environnement, Faculté des Sciences et techniques, Université Marien Ngouabi, Brazzaville, Congo.
    Zagidullina, Asiia
    Forest Research Institute, University of Quebec in Abitibi-Témiscamingue, QC, Canada; Department of Physical Geography and Environmental Management Problems, Institute of Geography, Russian Science Academy, Moscow, Russian Federation.
    Andersson, Tommi
    Kevo Subarctic Research Institute, Biodiversity Unit, University of Turku, Turku, Finland.
    Galiano-Cabrera, Darcy F.
    Asociación Civil Sin Fines De Lucro Para La Biodiversidad, Investigación Y Desarrollo Ambiental En Ecosistemas Tropicales (ABIDA), Urbanización Ucchullo Grande, Avenida Argentina F-9, Cusco, Peru; Facultad de Ciencias Biológicas, Universidad Nacional de San Antonio Abad del Cusco, Av. de La Cultura 773, Cusco, Cusco Province, Peru.
    Jiménez-Castillo, Mylthon
    Instituto de Ciencias Ambientales y Evolutivas, Universidad Austral de Chile, Campus Isla Teja, Valdivia, Chile.
    Churski, Marcin
    Mammal Research Institute, Polish Academy of Sciences, Ul. Stoczek 1, Białowieża, Poland.
    Gage, Shelley A.
    Centre for Horticultural Science, Queensland Alliance for Agriculture and Food Innovation, The University of Queensland, 47 Mayers Road, Nambour, Australia.
    Filippova, Nina
    Yugra State University, Chekhova street, 16, Khanty-Mansiysk, Russian Federation.
    Francisco, Kainana S.
    Institute of Pacific Islands Forestry, Pacific Southwest Research Station, USDA Forest Service, HI, Hilo, United States.
    Gaglianese-Woody, Morgan
    Appalchian State University, 572 Rivers Street, NC, Boone, United States.
    Iankoshvili, Giorgi
    Institute of Ecology, Ilia State University, 3/5 Cholokashvili Ave, Tbilisi, Georgia.
    Kaswamila, Mgeta Adidas
    Senckenberg Biodiversity and Climate Research Centre, Frankfurt, Germany.
    Lyatuu, Herman
    Reforest Africa, PO Box 5, Kilombero District, Mang’ula, Tanzania.
    Mampouya Wenina, Y.E.
    Ecole Nationale Supérieure d’Agronomie et de Foresterie, Université Marien Ngouabi, Brazzaville, Congo; Laboratoire de Biodiversité, de Gestion des Ecosystèmes et de l’Environnement, Faculté des Sciences et techniques, Université Marien Ngouabi, Brazzaville, Congo.
    Materu, Brayan
    Senckenberg Biodiversity and Climate Research Centre, Frankfurt, Germany.
    Mbemba, M.
    CongoPeat Project, Ecole Nationale Supérieure d’Agronomie et de Foresterie, Université Marien Ngouabi, Brazzaville, Congo.
    Moritz, Ruslan
    Siberian Institute of Plant Physiology and Biochemistry SB RAS, Lermontova str., 132, Irkutsk, Russian Federation.
    Orang, Karma
    Ugyen Wangchuk Institute for Forest Research and Training, Department of Forests and Park Services, Ministry of Energy and Natural Resources, Lamai Goempa, Bumthang, Bhutan.
    Plyusnin, Sergey
    Pitirim Sorokin Syktyvkar State University, 455 Oktyabrsky prosp., Syktyvkar, Russian Federation.
    Puma Vilca, Beisit L.
    Asociación Civil Sin Fines De Lucro Para La Biodiversidad, Investigación Y Desarrollo Ambiental En Ecosistemas Tropicales (ABIDA), Urbanización Ucchullo Grande, Avenida Argentina F-9, Cusco, Peru; Kevo Subarctic Research Institute, Biodiversity Unit, University of Turku, Turku, Finland.
    Rodríguez-Solís, Maria
    Escuela de Ingeniería Forestal, Tecnológico de Costa Rica, Cartago, Costa Rica.
    Šamonil, Pavel
    The Silva Tarouca Research Institute, Květnové náměstí 391, Průhonice, Czech Republic.
    Stępniak, Kinga M.
    Mammal Research Institute, Polish Academy of Sciences, Ul. Stoczek 1, Białowieża, Poland; Department of Ecology, Faculty of Biology, University of Warsaw, Żwirki i Wigury 101, Warsaw, Poland.
    Walsh, Seana K.
    Department of Science and Conservation, National Tropical Botanical Garden, 3530 Papalina Road, HI, Kalāheo, United States.
    Xu, Han
    Research Institute of Tropical Forestry, Chinese Academy of Forestry, Guangzhou, China.
    Metcalfe, Daniel B.
    Umeå universitet, Teknisk-naturvetenskapliga fakulteten, Institutionen för ekologi, miljö och geovetenskap. Department of Physical Geography and Ecosystem Science, Lund University, Lund, Sweden.
    The impact of insect herbivory on biogeochemical cycling in broadleaved forests varies with temperature2024Ingår i: Nature Communications, E-ISSN 2041-1723, Vol. 15, nr 1, artikel-id 6011Artikel i tidskrift (Refereegranskat)
    Abstract [en]

    Herbivorous insects alter biogeochemical cycling within forests, but the magnitude of these impacts, their global variation, and drivers of this variation remain poorly understood. To address this knowledge gap and help improve biogeochemical models, we established a global network of 74 plots within 40 mature, undisturbed broadleaved forests. We analyzed freshly senesced and green leaves for carbon, nitrogen, phosphorus and silica concentrations, foliar production and herbivory, and stand-level nutrient fluxes. We show more nutrient release by insect herbivores at non-outbreak levels in tropical forests than temperate and boreal forests, that these fluxes increase strongly with mean annual temperature, and that they exceed atmospheric deposition inputs in some localities. Thus, background levels of insect herbivory are sufficiently large to both alter ecosystem element cycling and influence terrestrial carbon cycling. Further, climate can affect interactions between natural populations of plants and herbivores with important consequences for global biogeochemical cycles across broadleaved forests.

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  • 15. Kristensen, Jeppe A.
    et al.
    Michelsen, Anders
    Metcalfe, Daniel B.
    Umeå universitet, Teknisk-naturvetenskapliga fakulteten, Institutionen för ekologi, miljö och geovetenskap. Department of Physical Geography and Ecosystem Science, Lund University, Lund, Sweden.
    Background insect herbivory increases with local elevation but makes minor contribution to element cycling along natural gradients in the Subarctic2020Ingår i: Ecology and Evolution, E-ISSN 2045-7758, Vol. 10, nr 20, s. 11684-11698Artikel i tidskrift (Refereegranskat)
    Abstract [en]

    Herbivores can exert major controls over biogeochemical cycling. As invertebrates are highly sensitive to temperature shifts (ectothermal), the abundances of insects in high-latitude systems, where climate warming is rapid, is expected to increase. In subarctic mountain birch forests, research has focussed on geometrid moth outbreaks, while the contribution of background insect herbivory (BIH) to elemental cycling is poorly constrained. In northern Sweden, we estimated BIH along 9 elevational gradients distributed across a gradient in regional elevation, temperature, and precipitation to allow evaluation of consistency in local versus regional variation. We converted foliar loss via BIH to fluxes of C, nitrogen (N), and phosphorus (P) from the birch canopy to the soil to compare with other relevant soil inputs of the same elements and assessed different abiotic and biotic drivers of the observed variability. We found that leaf area loss due to BIH was similar to 1.6% on average. This is comparable to estimates from tundra, but considerably lower than ecosystems at lower latitudes. The C, N, and P fluxes from canopy to soil associated with BIH were 1-2 orders of magnitude lower than the soil input from senesced litter and external nutrient sources such as biological N fixation, atmospheric deposition of N, and P weathering estimated from the literature. Despite the minor contribution to overall elemental cycling in subarctic birch forests, the higher quality and earlier timing of the input of herbivore deposits to soils compared to senesced litter may make this contribution disproportionally important for various ecosystem functions. BIH increased significantly with leaf N content as well as local elevation along each transect, yet showed no significant relationship with temperature or humidity, nor the commonly used temperature proxy, absolute elevation. The lack of consistency between the local and regional elevational trends calls for caution when using elevation gradients as climate proxies.

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  • 16.
    Prager, Case M.
    et al.
    Ecology and Evolutionary Biology Department, University of Michigan, MI, Ann Arbor, United States; The Rocky Mountain Biological Laboratory, CO, Crested Butte, United States.
    Classen, Aimee T.
    Ecology and Evolutionary Biology Department, University of Michigan, MI, Ann Arbor, United States; The Rocky Mountain Biological Laboratory, CO, Crested Butte, United States; Natural History Museum of Denmark, University of Copenhagen, Copenhagen, Denmark.
    Sundqvist, Maja K.
    Natural History Museum of Denmark, University of Copenhagen, Copenhagen, Denmark; Department of Forest Ecology and Management, Swedish University of Agricultural Sciences, Umeå, Sweden.
    Barrios-Garcia, Maria Noelia
    CONICET, CENAC-APN, Rio Negro, San Carlos de Bariloche, Argentina; Rubenstein School of Environment and Natural Resources, University of Vermont, VT, Burlington, United States.
    Cameron, Erin K.
    Department of Environmental Science, Saint Mary's University, NS, Halifax, Canada.
    Chen, Litong
    Qinghai Provincial Key Laboratory of Restoration Ecology of Cold Area and Key Laboratory of Adaptation and Evolution of Plant Biota, Northwest Institute of Plateau Biology, Chinese Academy of Sciences, Xining, China.
    Chisholm, Chelsea
    Department of Environment Systems Science, Institute of Integrative Biology, ETH Zürich, Zürich, Switzerland.
    Crowther, Thomas W.
    Department of Environment Systems Science, Institute of Integrative Biology, ETH Zürich, Zürich, Switzerland.
    Deslippe, Julie R.
    Centre for Biodiversity and Restoration Ecology, School of Biological Sciences, Victoria University of Wellington, Wellington, New Zealand.
    Grigulis, Karl
    Laboratoire d'Ecologie Alpine, Université Grenoble Alpes – CNRS – Université Savoie Mont-Blanc, Grenoble, France.
    He, Jin-Sheng
    Department of Ecology, College of Urban and Environmental Sciences, Peking University, Beijing, China.
    Henning, Jeremiah A.
    The Rocky Mountain Biological Laboratory, CO, Crested Butte, United States; Department of Biology, University of South Alabama, AL, Mobile, United States.
    Hovenden, Mark
    Biological Sciences, School of Natural Sciences, University of Tasmania, TAS, Hobart, Australia.
    Høye, Toke T. Thomas
    Department of Ecoscience and Arctic Research Centre, Aarhus University, Aarhus C, Denmark.
    Jing, Xin
    Natural History Museum of Denmark, University of Copenhagen, Copenhagen, Denmark; State Key Laboratory of Grassland Agro-Ecosystems, and College of Pastoral Agriculture Science and Technology, Lanzhou University, Gansu, Lanzhou, China.
    Lavorel, Sandra
    Laboratoire d'Ecologie Alpine, Université Grenoble Alpes – CNRS – Université Savoie Mont-Blanc, Grenoble, France.
    McLaren, Jennie R.
    Department of Biological Sciences, University of Texas at El Paso, TX, El Paso, United States.
    Metcalfe, Daniel B.
    Umeå universitet, Teknisk-naturvetenskapliga fakulteten, Institutionen för ekologi, miljö och geovetenskap.
    Newman, Gregory S.
    Department of Biology, University of Oklahoma, OK, Norman, United States.
    Nielsen, Marie Louise
    Department of Ecoscience and Arctic Research Centre, Aarhus University, Aarhus C, Denmark.
    Rixen, Christian
    Mountain Ecosystems Group, WSL Institute for Snow and Avalanche Research SLF, Davos Dorf, Switzerland.
    Read, Quentin D.
    The Rocky Mountain Biological Laboratory, CO, Crested Butte, United States; National Socio-Environmental Synthesis Center, MD, Annapolis, United States.
    Rewcastle, Kenna E.
    Rubenstein School of Environment and Natural Resources, University of Vermont, VT, Burlington, United States.
    Rodriguez-Cabal, Mariano
    Rubenstein School of Environment and Natural Resources, University of Vermont, VT, Burlington, United States; Grupo de Ecología de Invasiones, INIBIOMA, CONICET, Universidad Nacional del Comahue, San Carlos de Bariloche, Argentina.
    Wardle, David A.
    Asian School of the Environment, Nanyang Technological University, Singapore, Singapore.
    Wipf, Sonja
    Department of Biology, University of Oklahoma, OK, Norman, United States; Department of Research and Monitoring, Chastè Planta-Wildenberg, Zernez, Switzerland.
    Sanders, Nathan J.
    Ecology and Evolutionary Biology Department, University of Michigan, MI, Ann Arbor, United States; The Rocky Mountain Biological Laboratory, CO, Crested Butte, United States; Natural History Museum of Denmark, University of Copenhagen, Copenhagen, Denmark.
    Integrating natural gradients, experiments, and statistical modeling in a distributed network experiment: An example from the WaRM Network2022Ingår i: Ecology and Evolution, E-ISSN 2045-7758, Vol. 12, nr 10, artikel-id e9396Artikel i tidskrift (Refereegranskat)
    Abstract [en]

    A growing body of work examines the direct and indirect effects of climate change on ecosystems, typically by using manipulative experiments at a single site or performing meta-analyses across many independent experiments. However, results from single-site studies tend to have limited generality. Although meta-analytic approaches can help overcome this by exploring trends across sites, the inherent limitations in combining disparate datasets from independent approaches remain a major challenge. In this paper, we present a globally distributed experimental network that can be used to disentangle the direct and indirect effects of climate change. We discuss how natural gradients, experimental approaches, and statistical techniques can be combined to best inform predictions about responses to climate change, and we present a globally distributed experiment that utilizes natural environmental gradients to better understand long-term community and ecosystem responses to environmental change. The warming and (species) removal in mountains (WaRM) network employs experimental warming and plant species removals at high- and low-elevation sites in a factorial design to examine the combined and relative effects of climatic warming and the loss of dominant species on community structure and ecosystem function, both above- and belowground. The experimental design of the network allows for increasingly common statistical approaches to further elucidate the direct and indirect effects of warming. We argue that combining ecological observations and experiments along gradients is a powerful approach to make stronger predictions of how ecosystems will function in a warming world as species are lost, or gained, in local communities.

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  • 17.
    Roberts, Aradhana J.
    et al.
    Department of Physical Geography and Ecosystem Science, Lund University, Lund, Sweden.
    Crowley, Liam M.
    School of Biosciences, University of Birmingham, Edgbaston, Birmingham, United Kingdom; The Birmingham Institute of Forest Research, University of Birmingham, Edgbaston, Birmingham, United Kingdom.
    Sadler, Jon P.
    The Birmingham Institute of Forest Research, University of Birmingham, Edgbaston, Birmingham, United Kingdom; School of Geography, Earth and Environmental Sciences, University of Birmingham, Edgbaston, Birmingham, United Kingdom.
    Nguyen, Tien T. T.
    School of Biosciences, University of Birmingham, Edgbaston, Birmingham, United Kingdom.
    Hayward, Scott A. L.
    School of Biosciences, University of Birmingham, Edgbaston, Birmingham, United Kingdom; The Birmingham Institute of Forest Research, University of Birmingham, Edgbaston, Birmingham, United Kingdom.
    Metcalfe, Daniel B.
    Umeå universitet, Teknisk-naturvetenskapliga fakulteten, Institutionen för ekologi, miljö och geovetenskap. Department of Physical Geography and Ecosystem Science, Lund University, Lund, Sweden.
    Effects of Elevated Atmospheric CO2 Concentration on Insect Herbivory and Nutrient Fluxes in a Mature Temperate Forest2022Ingår i: Forests, E-ISSN 1999-4907, Vol. 13, nr 7, artikel-id 998Artikel i tidskrift (Refereegranskat)
    Abstract [en]

    Insect herbivory is one of the most important ecological processes affecting plant–soil feedbacks and overall forest ecosystem health. In this study, we assess how elevated carbon dioxide (eCO2) impacts (i) leaf level insect herbivory and (ii) the stand-level herbivore-mediated transfer of carbon (C) and nitrogen (N) from the canopy to the ground in a natural mature oak temperate forest community in central England at the Birmingham Institute of Forest Research Free Air CO2 Enrichment (BIFoR FACE) site. Recently abscised leaves were collected every two weeks through the growing season in August to December from 2017–2019, with the identification of four dominant species: Quercus robur (pedunculate oak), Acer pseudoplatanus (sycamore), Crataegus monogyna (com-mon hawthorn) and Corylus avellana (hazel). The selected leaves were scanned and visually analyzed to quantify the leaf area loss from folivory monthly. Additionally, the herbivore-mediated transfer of C and N fluxes from the dominant tree species Q. robur was calculated from these leaf-level folivory estimates, the total foliar production and the foliar C and N contents. This study finds that the leaf-level herbivory at the BIFoR FACE has not changed significantly across the first 3 years of eCO2 treatment when assessed across all dominant tree species, although we detected significant changes under the eCO2 treatment for individual tree species and years. Despite the lack of any strong leaf-level herbivory response, the estimated stand-level foliar C and N transferred to the ground via herbivory was substantially higher under eCO2, mainly because there was a ~50% increase in the foliar production of Q. robur under eCO2. This result cautions against concluding much from either the presence or absence of leaf-level herbivory responses to any environmental effect, because their actual ecosystem effects are filtered through so many (usually unmeasured) factors.

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  • 18.
    Smith, Melinda D.
    et al.
    Department of Biology, Colorado State University, Fort Collins, United States; Graduate Degree Program in Ecology, Colorado State University, Fort Collins, United States.
    Metcalfe, Daniel B.
    Umeå universitet, Teknisk-naturvetenskapliga fakulteten, Institutionen för ekologi, miljö och geovetenskap.
    Zuo, Xiaoan
    Urat Desert-grassland Research Station, Northwest Institute of Eco-Environment and Resources, Chinese Academy of Science, Lanzhou, China.
    Extreme drought impacts have been underestimated in grasslands and shrublands globally2024Ingår i: Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, E-ISSN 1091-6490, Vol. 121, nr 4, artikel-id e2309881120Artikel i tidskrift (Refereegranskat)
    Abstract [en]

    Climate change is increasing the frequency and severity of short-term (~1 y) drought events-the most common duration of drought-globally. Yet the impact of this intensification of drought on ecosystem functioning remains poorly resolved. This is due in part to the widely disparate approaches ecologists have employed to study drought, variation in the severity and duration of drought studied, and differences among ecosystems in vegetation, edaphic and climatic attributes that can mediate drought impacts. To overcome these problems and better identify the factors that modulate drought responses, we used a coordinated distributed experiment to quantify the impact of short-term drought on grassland and shrubland ecosystems. With a standardized approach, we imposed ~a single year of drought at 100 sites on six continents. Here we show that loss of a foundational ecosystem function-aboveground net primary production (ANPP)-was 60% greater at sites that experienced statistically extreme drought (1-in-100-y event) vs. those sites where drought was nominal (historically more common) in magnitude (35% vs. 21%, respectively). This reduction in a key carbon cycle process with a single year of extreme drought greatly exceeds previously reported losses for grasslands and shrublands. Our global experiment also revealed high variability in drought response but that relative reductions in ANPP were greater in drier ecosystems and those with fewer plant species. Overall, our results demonstrate with unprecedented rigor that the global impacts of projected increases in drought severity have been significantly underestimated and that drier and less diverse sites are likely to be most vulnerable to extreme drought.

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  • 19.
    Soininen, E.M.
    et al.
    Department of Arctic and Marine Biology, UiT-The Arctic University of Norway, Tromsø, Norway.
    Barrio, I.C.
    Faculty of Environmental and Forest Sciences, Agricultural University of Iceland, Keldnaholt, Reykjavík, Iceland.
    Bjørkås, R.
    Centre for Biodiversity Dynamics, Department of Biology, Norwegian University of Science and Technology, Trondheim, Norway; Centre for Ecological and Evolutionary Synthesis, University of Oslo, Oslo, Norway.
    Björnsdóttir, K.
    Department of Biological and Environmental Sciences, University of Gothenburg, PO Box 461, Gothenburg, Sweden.
    Ehrich, D.
    Department of Arctic and Marine Biology, UiT-The Arctic University of Norway, Tromsø, Norway.
    Hopping, K.A.
    Human-Environment Systems, Boise State University, ID, Boise, United States.
    Kaarlejärvi, E.
    Organismal and Evolutionary Research Programme, University of Helsinki, Helsinki, Finland.
    Kolstad, A.L.
    Department of Natural History, NTNU University Museum, Norwegian University of Science and Technology, Trondheim, Norway.
    Abdulmanova, S.
    Dynamics of Arctic Ecosystems Lab, Arctic Research Station, Institute of Plant and Animal Ecology Ural Branch of Russian Academy of Sciences, Zelenaya Gorka Str., 21, Labytnangi, Russian Federation.
    Björk, R.G.
    Department of Earth Sciences, University of Gothenburg, Gothenburg, Sweden; Gothenburg Global Biodiversity Centre, Gothenburg, Sweden.
    Bueno, C.G.
    Department of Botany, Institute of Ecology and Earth Sciences, University of Tartu, Tartu, Estonia.
    Eischeid, I.
    Department of Arctic and Marine Biology, UiT-The Arctic University of Norway, Tromsø, Norway; Norwegian Polar Institute, Fram Centre, Tromsø, Norway.
    Finger-Higgens, R.
    Ecology, Evolution, Ecosystems and Society, Dartmouth College, NH, Hanover, United States.
    Forbey, J.S.
    Department of Biological Sciences, Boise State University, ID, Boise, United States.
    Gignac, C.
    Centre d’études Nordiques and Plant Science Department, Université Laval, 2425 rue de l’Agriculture, QC, Québec City, Canada.
    Gilg, O.
    UMR 6249 Chrono-Environnement, Université de Bourgogne Franche-Comté, Besançon, France; Groupe de Recherche en Ecologie Arctique, Francheville, France.
    den Herder, M.
    European Forest Institute, Yliopistokatu 6 B, Joensuu, Finland.
    Holm, H.S.
    Department of Arctic and Marine Biology, UiT-The Arctic University of Norway, Tromsø, Norway.
    Hwang, B.C.
    Department of Physical Geography and Ecosystem Science, Lund University, Sölvegaten 12, Lund, Sweden.
    Jepsen, J.U.
    Department of Arctic Ecology, Norwegian Institute for Nature Research, Fram Centre, Tromsø, Norway.
    Kamenova, S.
    Department of Natural History, NTNU University Museum, Norwegian University of Science and Technology, Trondheim, Norway; Centre for Ecological and Evolutionary Synthesis, University of Oslo, Oslo, Norway.
    Kater, I.
    Department of Biosciences, University of Durham, Stockton Road, Durham, United Kingdom.
    Koltz, A.M.
    Department of Biology, Washington University in St. Louis, MO, St. Louis, United States; The Arctic Institute, DC, Washington, United States.
    Kristensen, J.A.
    Department of Physical Geography and Ecosystem Science, Lund University, Sölvegaten 12, Lund, Sweden; School of Geography and the Environment, University of Oxford, Oxford, United Kingdom.
    Little, C.J.
    School of Environmental Science, Simon Fraser University, BC, Burnaby, Canada.
    Macek, P.
    Institute of Hydrobiology, Biology Centre of Czech Academy of Sciences, Na Sadkach 7, Ceske Budejovice, Czech Republic; Faculty of Science, University of South Bohemia, Branisovska 1760, Ceske Budejovice, Czech Republic.
    Mathisen, K.M.
    Department of Forestry and Wildlife Management, Inland Norway University of Applied Sciences, Elverum, Norway.
    Metcalfe, Daniel B.
    Umeå universitet, Teknisk-naturvetenskapliga fakulteten, Institutionen för ekologi, miljö och geovetenskap. Department of Physical Geography and Ecosystem Science, Lund University, Lund, Sweden.
    Mosbacher, J.B.
    Norwegian Polar Institute, Fram Centre, Tromsø, Norway.
    Mörsdorf, M.
    Department of Biology, University of Freiburg, Freiburg, Germany.
    Park, T.
    NASA Ames Research Center, CA, Moffett Field, United States; Bay Area Environmental Research Institute, CA, Moffett Field, United States.
    Propster, J.R.
    Center for Ecosystem Science and Society, Northern Arizona University, AZ, Flagstaff, United States; Department of Biological Sciences, Northern Arizona University, AZ, Flagstaff, United States.
    Roberts, A.J.
    Department of Physical Geography and Ecosystem Science, Lund University, Sölvegaten 12, Lund, Sweden.
    Serrano, E.
    Wildlife Ecology and Health Group (WE&H) and Servei d’Ecopatologia de Fauna Salvatge (SEFaS), Departament de Medicina I Cirurgia Animals, Universitat Autònoma de Barcelona, Bellaterra, Barcelona, Spain.
    Spiegel, M.P.
    School of Geography and the Environment, University of Oxford, Oxford, United Kingdom.
    Tamayo, M.
    Environment and Natural Resources, University of Iceland, Sturlugata 7, 101, Reykjavík, Iceland.
    Tuomi, M.W.
    Department of Arctic and Marine Biology, UiT-The Arctic University of Norway, Tromsø, Norway.
    Verma, M.
    Institute of Zoology, Zoological Society of London, Regent’s Park, London, United Kingdom.
    Vuorinen, K.E.M.
    Department of Natural History, NTNU University Museum, Norwegian University of Science and Technology, Trondheim, Norway.
    Väisänen, M.
    Ecology and Genetics Research Unit, University of Oulu, P. O. Box 3000, Oulu, Finland; Arctic Centre, University of Lapland, P. O. Box 122, Rovaniemi, Finland.
    van der Wal, R.
    Department of Ecology, Swedish University of Agricultural Sciences (SLU), Ulls väg 16, Uppsala, Sweden.
    Wilcots, M.E.
    Department of Ecology, Evolution, and Behavior, University of Minnesota, 140 Gortner Laboratory, 1479 Gortner Ave., MN, St. Paul, United States.
    Yoccoz, N.G.
    Department of Arctic and Marine Biology, UiT-The Arctic University of Norway, Tromsø, Norway.
    Speed, J.D.M.
    Department of Natural History, NTNU University Museum, Norwegian University of Science and Technology, Trondheim, Norway.
    Location of studies and evidence of effects of herbivory on Arctic vegetation: a systematic map2021Ingår i: Environmental Evidence, E-ISSN 2047-2382, Vol. 10, nr 1, artikel-id 25Artikel i tidskrift (Refereegranskat)
    Abstract [en]

    Background: Herbivores modify the structure and function of tundra ecosystems. Understanding their impacts is necessary to assess the responses of these ecosystems to ongoing environmental changes. However, the effects of herbivores on plants and ecosystem structure and function vary across the Arctic. Strong spatial variation in herbivore effects implies that the results of individual studies on herbivory depend on local conditions, i.e., their ecological context. An important first step in assessing whether generalizable conclusions can be produced is to identify the existing studies and assess how well they cover the underlying environmental conditions across the Arctic. This systematic map aims to identify the ecological contexts in which herbivore impacts on vegetation have been studied in the Arctic. Specifically, the primary question of the systematic map was: “What evidence exists on the effects of herbivores on Arctic vegetation?”.

    Methods: We used a published systematic map protocol to identify studies addressing the effects of herbivores on Arctic vegetation. We conducted searches for relevant literature in online databases, search engines and specialist websites. Literature was screened to identify eligible studies, defined as reporting primary data on herbivore impacts on Arctic plants and plant communities. We extracted information on variables that describe the ecological context of the studies, from the studies themselves and from geospatial data. We synthesized the findings narratively and created a Shiny App where the coded data are searchable and variables can be visually explored.

    Review findings: We identified 309 relevant articles with 662 studies (representing different ecological contexts or datasets within the same article). These studies addressed vertebrate herbivory seven times more often than invertebrate herbivory. Geographically, the largest cluster of studies was in Northern Fennoscandia. Warmer and wetter parts of the Arctic had the largest representation, as did coastal areas and areas where the increase in temperature has been moderate. In contrast, studies spanned the full range of ecological context variables describing Arctic vertebrate herbivore diversity and human population density and impact.

    Conclusions: The current evidence base might not be sufficient to understand the effects of herbivores on Arctic vegetation throughout the region, as we identified clear biases in the distribution of herbivore studies in the Arctic and a limited evidence base on invertebrate herbivory. In particular, the overrepresentation of studies in areas with moderate increases in temperature prevents robust generalizations about the effects of herbivores under different climatic scenarios.

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  • 20.
    Ylänne, Henni
    et al.
    Centre for Environmental and Climate Science, Lund University, Lund, Sweden.
    Madsen, Rieke L.
    Department of Biology, Lund University, Lund, Sweden.
    Castaño, Carles
    Uppsala BioCenter, Department of Forest Mycology and Plant Pathology, Swedish University of Agricultural Sciences, Uppsala, Sweden.
    Metcalfe, Daniel B.
    Umeå universitet, Teknisk-naturvetenskapliga fakulteten, Institutionen för ekologi, miljö och geovetenskap. Department of Physical Geography and Ecosystem Science, Lund University, Lund, Sweden.
    Clemmensen, Karina E.
    Uppsala BioCenter, Department of Forest Mycology and Plant Pathology, Swedish University of Agricultural Sciences, Uppsala, Sweden.
    Reindeer control over subarctic treeline alters soil fungal communities with potential consequences for soil carbon storage2021Ingår i: Global Change Biology, ISSN 1354-1013, E-ISSN 1365-2486, Vol. 27, nr 18, s. 4254-4268Artikel i tidskrift (Refereegranskat)
    Abstract [en]

    The climate-driven encroachment of shrubs into the Arctic is accompanied by shifts in soil fungal communities that could contribute to a net release of carbon from tundra soils. At the same time, arctic grazers are known to prevent the establishment of deciduous shrubs and, under certain conditions, promote the dominance of evergreen shrubs. As these different vegetation types associate with contrasting fungal communities, the belowground consequences of climate change could vary among grazing regimes. Yet, at present, the impact of grazing on soil fungal communities and their links to soil carbon have remained speculative. Here we tested how soil fungal community composition, diversity and function depend on tree vicinity and long-term reindeer grazing regime and assessed how the fungal communities relate to organic soil carbon stocks in an alpine treeline ecotone in Northern Scandinavia. We determined soil carbon stocks and characterized soil fungal communities directly underneath and >3 m away from mountain birches (Betula pubescens ssp. czerepanovii) in two adjacent 55-year-old grazing regimes with or without summer grazing by reindeer (Rangifer tarandus). We show that the area exposed to year-round grazing dominated by evergreen dwarf shrubs had higher soil C:N ratio, higher fungal abundance and lower fungal diversity compared with the area with only winter grazing and higher abundance of mountain birch. Although soil carbon stocks did not differ between the grazing regimes, stocks were positively associated with root-associated ascomycetes, typical to the year-round grazing regime, and negatively associated with free-living saprotrophs, typical to the winter grazing regime. These findings suggest that when grazers promote dominance of evergreen dwarf shrubs, they induce shifts in soil fungal communities that increase soil carbon sequestration in the long term. Thus, to predict climate-driven changes in soil carbon, grazer-induced shifts in vegetation and soil fungal communities need to be accounted for.

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