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  • image/svg+xml art designer at PLoS, modified by Wikipedia users Nina, Beao, JakobVoss, and AnonMoos Open Access logo, converted into svg, designed by PLoS. This version with transparent background. http://commons.wikimedia.org/wiki/File:Open_Access_logo_PLoS_white.svg art designer at PLoS, modified by Wikipedia users Nina, Beao, JakobVoss, and AnonMoos http://www.plos.org/
    Authors: Lembrechts, Jonas J; Van Den Hoogen, Johan; Aalto, Juha; Ashcroft, Michael B; +196 Authors

    AbstractResearch in global change ecology relies heavily on global climatic grids derived from estimates of air temperature in open areas at around 2 m above the ground. These climatic grids do not reflect conditions below vegetation canopies and near the ground surface, where critical ecosystem functions occur and most terrestrial species reside. Here, we provide global maps of soil temperature and bioclimatic variables at a 1‐km2resolution for 0–5 and 5–15 cm soil depth. These maps were created by calculating the difference (i.e. offset) between in situ soil temperature measurements, based on time series from over 1200 1‐km2pixels (summarized from 8519 unique temperature sensors) across all the world's major terrestrial biomes, and coarse‐grained air temperature estimates from ERA5‐Land (an atmospheric reanalysis by the European Centre for Medium‐Range Weather Forecasts). We show that mean annual soil temperature differs markedly from the corresponding gridded air temperature, by up to 10°C (mean = 3.0 ± 2.1°C), with substantial variation across biomes and seasons. Over the year, soils in cold and/or dry biomes are substantially warmer (+3.6 ± 2.3°C) than gridded air temperature, whereas soils in warm and humid environments are on average slightly cooler (−0.7 ± 2.3°C). The observed substantial and biome‐specific offsets emphasize that the projected impacts of climate and climate change on near‐surface biodiversity and ecosystem functioning are inaccurately assessed when air rather than soil temperature is used, especially in cold environments. The global soil‐related bioclimatic variables provided here are an important step forward for any application in ecology and related disciplines. Nevertheless, we highlight the need to fill remaining geographic gaps by collecting more in situ measurements of microclimate conditions to further enhance the spatiotemporal resolution of global soil temperature products for ecological applications.

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    image/svg+xml art designer at PLoS, modified by Wikipedia users Nina, Beao, JakobVoss, and AnonMoos Open Access logo, converted into svg, designed by PLoS. This version with transparent background. http://commons.wikimedia.org/wiki/File:Open_Access_logo_PLoS_white.svg art designer at PLoS, modified by Wikipedia users Nina, Beao, JakobVoss, and AnonMoos http://www.plos.org/
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    image/svg+xml art designer at PLoS, modified by Wikipedia users Nina, Beao, JakobVoss, and AnonMoos Open Access logo, converted into svg, designed by PLoS. This version with transparent background. http://commons.wikimedia.org/wiki/File:Open_Access_logo_PLoS_white.svg art designer at PLoS, modified by Wikipedia users Nina, Beao, JakobVoss, and AnonMoos http://www.plos.org/
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    Global Change Biology
    Article . 2022 . Peer-reviewed
    License: CC BY NC
    Data sources: Crossref
    image/svg+xml art designer at PLoS, modified by Wikipedia users Nina, Beao, JakobVoss, and AnonMoos Open Access logo, converted into svg, designed by PLoS. This version with transparent background. http://commons.wikimedia.org/wiki/File:Open_Access_logo_PLoS_white.svg art designer at PLoS, modified by Wikipedia users Nina, Beao, JakobVoss, and AnonMoos http://www.plos.org/
    Global Change Biology
    Article
    License: implied-oa
    Data sources: UnpayWall
    image/svg+xml art designer at PLoS, modified by Wikipedia users Nina, Beao, JakobVoss, and AnonMoos Open Access logo, converted into svg, designed by PLoS. This version with transparent background. http://commons.wikimedia.org/wiki/File:Open_Access_logo_PLoS_white.svg art designer at PLoS, modified by Wikipedia users Nina, Beao, JakobVoss, and AnonMoos http://www.plos.org/
    https://doi.org/10.32942/osf.i...
    Article . 2021 . Peer-reviewed
    License: CC BY SA
    Data sources: Crossref
    image/svg+xml art designer at PLoS, modified by Wikipedia users Nina, Beao, JakobVoss, and AnonMoos Open Access logo, converted into svg, designed by PLoS. This version with transparent background. http://commons.wikimedia.org/wiki/File:Open_Access_logo_PLoS_white.svg art designer at PLoS, modified by Wikipedia users Nina, Beao, JakobVoss, and AnonMoos http://www.plos.org/
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    Research Collection
    Article . 2022
    License: CC BY NC
    Data sources: Datacite
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    https://dx.doi.org/10.5445/ir/...
    Article . 2022
    License: CC BY NC
    Data sources: Datacite
    image/svg+xml art designer at PLoS, modified by Wikipedia users Nina, Beao, JakobVoss, and AnonMoos Open Access logo, converted into svg, designed by PLoS. This version with transparent background. http://commons.wikimedia.org/wiki/File:Open_Access_logo_PLoS_white.svg art designer at PLoS, modified by Wikipedia users Nina, Beao, JakobVoss, and AnonMoos http://www.plos.org/
    https://dx.doi.org/10.21256/zh...
    Article . 2022
    License: CC BY NC
    Data sources: Datacite
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    image/svg+xml art designer at PLoS, modified by Wikipedia users Nina, Beao, JakobVoss, and AnonMoos Open Access logo, converted into svg, designed by PLoS. This version with transparent background. http://commons.wikimedia.org/wiki/File:Open_Access_logo_PLoS_white.svg art designer at PLoS, modified by Wikipedia users Nina, Beao, JakobVoss, and AnonMoos http://www.plos.org/
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    ZENODO
    Article . 2022
    License: CC BY
    Data sources: ZENODO
    image/svg+xml art designer at PLoS, modified by Wikipedia users Nina, Beao, JakobVoss, and AnonMoos Open Access logo, converted into svg, designed by PLoS. This version with transparent background. http://commons.wikimedia.org/wiki/File:Open_Access_logo_PLoS_white.svg art designer at PLoS, modified by Wikipedia users Nina, Beao, JakobVoss, and AnonMoos http://www.plos.org/
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    Research Collection
    Article . 2022
    License: CC BY NC
    image/svg+xml art designer at PLoS, modified by Wikipedia users Nina, Beao, JakobVoss, and AnonMoos Open Access logo, converted into svg, designed by PLoS. This version with transparent background. http://commons.wikimedia.org/wiki/File:Open_Access_logo_PLoS_white.svg art designer at PLoS, modified by Wikipedia users Nina, Beao, JakobVoss, and AnonMoos http://www.plos.org/
    Wageningen Staff Publications
    Article . 2022
    License: CC BY NC
    image/svg+xml art designer at PLoS, modified by Wikipedia users Nina, Beao, JakobVoss, and AnonMoos Open Access logo, converted into svg, designed by PLoS. This version with transparent background. http://commons.wikimedia.org/wiki/File:Open_Access_logo_PLoS_white.svg art designer at PLoS, modified by Wikipedia users Nina, Beao, JakobVoss, and AnonMoos http://www.plos.org/
    Munin - Open Research Archive
    Article . 2021 . Peer-reviewed
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    Munin - Open Research Archive
    Article . 2021 . Peer-reviewed
    License: CC BY
    image/svg+xml art designer at PLoS, modified by Wikipedia users Nina, Beao, JakobVoss, and AnonMoos Open Access logo, converted into svg, designed by PLoS. This version with transparent background. http://commons.wikimedia.org/wiki/File:Open_Access_logo_PLoS_white.svg art designer at PLoS, modified by Wikipedia users Nina, Beao, JakobVoss, and AnonMoos http://www.plos.org/
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    Apollo
    Article . 2022
    Data sources: Datacite
    CNR ExploRA
    Article . 2022
    Data sources: CNR ExploRA
    Access Routes
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      image/svg+xml art designer at PLoS, modified by Wikipedia users Nina, Beao, JakobVoss, and AnonMoos Open Access logo, converted into svg, designed by PLoS. This version with transparent background. http://commons.wikimedia.org/wiki/File:Open_Access_logo_PLoS_white.svg art designer at PLoS, modified by Wikipedia users Nina, Beao, JakobVoss, and AnonMoos http://www.plos.org/ COREarrow_drop_down
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      Global Change Biology
      Article . 2022 . Peer-reviewed
      License: CC BY NC
      Data sources: Crossref
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      Global Change Biology
      Article
      License: implied-oa
      Data sources: UnpayWall
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      https://doi.org/10.32942/osf.i...
      Article . 2021 . Peer-reviewed
      License: CC BY SA
      Data sources: Crossref
      image/svg+xml art designer at PLoS, modified by Wikipedia users Nina, Beao, JakobVoss, and AnonMoos Open Access logo, converted into svg, designed by PLoS. This version with transparent background. http://commons.wikimedia.org/wiki/File:Open_Access_logo_PLoS_white.svg art designer at PLoS, modified by Wikipedia users Nina, Beao, JakobVoss, and AnonMoos http://www.plos.org/
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      Research Collection
      Article . 2022
      License: CC BY NC
      Data sources: Datacite
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      https://dx.doi.org/10.5445/ir/...
      Article . 2022
      License: CC BY NC
      Data sources: Datacite
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      https://dx.doi.org/10.21256/zh...
      Article . 2022
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      ZENODO
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      Research Collection
      Article . 2022
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      Wageningen Staff Publications
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      Munin - Open Research Archive
      Article . 2021 . Peer-reviewed
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      Munin - Open Research Archive
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      Apollo
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      CNR ExploRA
      Article . 2022
      Data sources: CNR ExploRA
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    Authors: Mariana García Criado; Isla H. Myers-Smith; Anne D. Bjorkman; Signe Normand; +37 Authors

    Climate change is leading to a species redistributions. In the tundra biome, many shrub species are expanding into new areas, a process known as shrubification. However, not all tundra shrub species will benefit from warming. Winner and loser species (those projected to expand and contract their ranges, and/or those that have increased or decreased in cover over time), and the characteristics that may determine success or failure, have not been fully identified. Here, we investigate whether current range sizes are related to plant trait values and intraspecific trait variation by combining 17,921 trait records and distribution data from 62 shrub species across three continents (>30 degrees north). In addition, we determine which traits are associated with species projected by species distribution models to expand or contract their ranges under climate change, and species that have undergone past cover changes over time. Winner and loser shrub species identified from projected range shifts generally differed from those identified from observed past cover change. We found that greater variation in seed mass and specific leaf area were related to larger projected range shifts. Projected winner species generally had greater seed mass values than ‘no change’ and loser species. However, contrary to our expectations, traits’ values and variation were not consistently related to current and projected ranges, and depended upon the future climate scenarios considered in range projections. There were no clear relationships either between cover change over time and trait values or variation. Overall, our findings indicate that abundance changes and projected range shifts will not lead to directional modifications in shrub trait composition or variation with future warming, since winner and loser species share relatively similar trait spaces based on commonly measured traits. Future research could investigate other morpho-physiological traits underpinning climatic preferences, which might better predict future range and abundance changes.

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    Nature Communications
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    Nature Communications
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    https://doi.org/10.32942/x23s3...
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      Nature Communications
      Article . 2023 . Peer-reviewed
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      Nature Communications
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      https://doi.org/10.32942/x23s3...
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    Authors: Isla H. Myers‐Smith; Haydn J. D. Thomas; Anne D. Bjorkman;

    Contents Summary 1742 I. Introduction 1742 II. The global context of tundra trait variation 1743 III. The current state of knowledge on trait change in the tundra biome 1744 IV. The links between traits and ecosystem functions 1744 V. Future priorities for tundra trait research 1746 VI. Conclusions 1746 References 1747 SummaryIn the rapidly warming tundra biome, plant traits provide an essential link between ongoing vegetation change and feedbacks to key ecosystem functions. However, only recently have comprehensive trait data been compiled for tundra species and sites, allowing us to assess key elements of functional responses to global change. In this review, we summarize trait‐based research in tundra ecosystems, with a focus on three components: plant trait variation and how it compares with global patterns; shifts in community‐level traits in response to environmental change; and the use of traits to understand and predict ecosystem function. Quantifying patterns and trends in plant traits will allow us to better project the consequences of environmental change for the ecology and functioning of tundra ecosystems.

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    New Phytologist
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    New Phytologist
    Article . 2018 . Peer-reviewed
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      New Phytologist
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      New Phytologist
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      Article . 2020
  • Authors: Dov F. Sax; Antoine Becker-Scarpitta; Jenny L. McCune; Isla H. Myers-Smith; +4 Authors

    Plant communities have undergone dramatic changes in recent centuries, although not all such changes fit with the dominant biodiversity-crisis narrative used to describe them. At the global scale, future declines in plant species diversity are highly likely given habitat conversion in the tropics, although few extinctions have been documented for the Anthropocene to date (<0.1%). Nonnative species introductions have greatly increased plant species richness in many regions of the world at the same time that they have led to the creation of new hybrid polyploid species by bringing previously isolated congeners into close contact. At the local scale, conversion of primary vegetation to agriculture has decreased plant diversity, whereas other drivers of change—e.g., climate warming, habitat fragmentation, and nitrogen deposition—have highly context-dependent effects, resulting in a distribution of temporal trends with a mean close to zero. These results prompt a reassessment of how conservation goals are defined and justified.

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    Authors: Logan T. Berner; Richard Massey; Patrick Jantz; Bruce C. Forbes; +10 Authors

    AbstractArctic warming can influence tundra ecosystem function with consequences for climate feedbacks, wildlife and human communities. Yet ecological change across the Arctic tundra biome remains poorly quantified due to field measurement limitations and reliance on coarse-resolution satellite data. Here, we assess decadal changes in Arctic tundra greenness using time series from the 30 m resolution Landsat satellites. From 1985 to 2016 tundra greenness increased (greening) at ~37.3% of sampling sites and decreased (browning) at ~4.7% of sampling sites. Greening occurred most often at warm sampling sites with increased summer air temperature, soil temperature, and soil moisture, while browning occurred most often at cold sampling sites that cooled and dried. Tundra greenness was positively correlated with graminoid, shrub, and ecosystem productivity measured at field sites. Our results support the hypothesis that summer warming stimulated plant productivity across much, but not all, of the Arctic tundra biome during recent decades.

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    Nature Communications
    Article . 2020 . Peer-reviewed
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    Nature Communications
    Article . 2020
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    Authors: Jelte Rozema; Ken D. Tape; Niels Martin Schmidt; Susanna Venn; +29 Authors

    Abstract Recent research using repeat photography, long-term ecological monitoring and dendrochronology has documented shrub expansion in arctic, high-latitude and alpine tundra ecosystems. Here, we (1) synthesize these findings, (2) present a conceptual framework that identifies mechanisms and constraints on shrub increase, (3) explore causes, feedbacks and implications of the increased shrub cover in tundra ecosystems, and (4) address potential lines of investigation for future research. Satellite observations from around the circumpolar Arctic, showing increased productivity, measured as changes in ‘greenness’, have coincided with a general rise in high-latitude air temperatures and have been partly attributed to increases in shrub cover. Studies indicate that warming temperatures, changes in snow cover, altered disturbance regimes as a result of permafrost thaw, tundra fires, and anthropogenic activities or changes in herbivory intensity are all contributing to observed changes in shrub abundance. A large-scale increase in shrub cover will change the structure of tundra ecosystems and alter energy fluxes, regional climate, soil–atmosphere exchange of water, carbon and nutrients, and ecological interactions between species. In order to project future rates of shrub expansion and understand the feedbacks to ecosystem and climate processes, future research should investigate the species or trait-specific responses of shrubs to climate change including: (1) the temperature sensitivity of shrub growth, (2) factors controlling the recruitment of new individuals, and (3) the relative influence of the positive and negative feedbacks involved in shrub expansion.

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    Environmental Research Letters
    Article . 2011 . Peer-reviewed
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    Authors: Mark Vellend; Carissa D. Brown; Heather M. Kharouba; Isla H. Myers-Smith; +1 Authors

    Predicting the future ecological impact of global change drivers requires understanding how these same drivers have acted in the past to produce the plant populations and communities we see today. Historical ecological data sources have made contributions of central importance to global change biology, but remain outside the toolkit of most ecologists. Here we review the strengths and weaknesses of four unconventional sources of historical ecological data: land survey records, “legacy” vegetation data, historical maps and photographs, and herbarium specimens. We discuss recent contributions made using these data sources to understanding the impacts of habitat disturbance and climate change on plant populations and communities, and the duration of extinction–colonization time lags in response to landscape change. Historical data frequently support inferences made using conventional ecological studies (e.g., increases in warm‐adapted species as temperature rises), but there are cases when the addition of different data sources leads to different conclusions (e.g., temporal vegetation change not as predicted by chronosequence studies). The explicit combination of historical and contemporary data sources is an especially powerful approach for unraveling long‐term consequences of multiple drivers of global change. Despite the limitations of historical data, which include spotty and potentially biased spatial and temporal coverage, they often represent the only means of characterizing ecological phenomena in the past and have proven indispensable for characterizing the nature, magnitude, and generality of global change impacts on plant populations and communities.

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    American Journal of Botany
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      American Journal of Botany
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  • Authors: Daskalova, Gergana; Myers-Smith, Isla; Bowler, Diana; Dornelas, Maria; +7 Authors

    Our aim is to quantify how global change drivers influence species’ populations and biodiversity change. Specifically, we will focus on the effects of climate change, human use, human population density, pollution and invasion pressure on temporal changes in population abundance, species richness and community composition (turnover), as these drivers capture the variety of ways in which humans are altering the planet. We will test if the individual, cumulative and interactive effects of the different types of global change explain the heterogeneous patterns of population and biodiversity change observed across the planet.

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    Authors: Callaghan, Terry V.; Tweedie, Craig E.; Åkerman, Jonas; Andrews, Christopher; +49 Authors

    Understanding the responses of tundra systems to global change has global implications. Most tundra regions lack sustained environmental monitoring and one of the only ways to document multi-decadal change is to resample historic research sites. The International Polar Year (IPY) provided a unique opportunity for such research through the Back to the Future (BTF) project (IPY project #512). This article synthesizes the results from 13 papers within this Ambio Special Issue. Abiotic changes include glacial recession in the Altai Mountains, Russia; increased snow depth and hardness, permafrost warming, and increased growing season length in sub-arctic Sweden; drying of ponds in Greenland; increased nutrient availability in Alaskan tundra ponds, and warming at most locations studied. Biotic changes ranged from relatively minor plant community change at two sites in Greenland to moderate change in the Yukon, and to dramatic increases in shrub and tree density on Herschel Island, and in subarctic Sweden. The population of geese tripled at one site in northeast Greenland where biomass in non-grazed plots doubled. A model parameterized using results from a BTF study forecasts substantial declines in all snowbeds and increases in shrub tundra on Niwot Ridge, Colorado over the next century. In general, results support and provide improved capacities for validating experimental manipulation, remote sensing, and modeling studies.

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    AMBIO
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    Authors: Daskalova, Gergana N.; Myers-Smith, Isla H.; Godlee, John L.;

    AbstractThe Earth’s biota is changing over time in complex ways. A critical challenge is to test whether specific biomes, taxa or types of species benefit or suffer in a time of accelerating global change. We analysed nearly 10,000 abundance time series from over 2000 vertebrate species part of the Living Planet Database. We integrated abundance data with information on geographic range, habitat preference, taxonomic and phylogenetic relationships, and IUCN Red List Categories and threats. We find that 15% of populations declined, 18% increased, and 67% showed no net changes over time. Against a backdrop of no biogeographic and phylogenetic patterning in population change, we uncover a distinct taxonomic signal. Amphibians were the only taxa that experienced net declines in the analysed data, while birds, mammals and reptiles experienced net increases. Population trends were poorly captured by species’ rarity and global-scale threats. Incorporation of the full spectrum of population change will improve conservation efforts to protect global biodiversity.

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    Nature Communications
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    https://doi.org/10.1101/272898...
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      Nature Communications
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      https://doi.org/10.1101/272898...
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  • image/svg+xml art designer at PLoS, modified by Wikipedia users Nina, Beao, JakobVoss, and AnonMoos Open Access logo, converted into svg, designed by PLoS. This version with transparent background. http://commons.wikimedia.org/wiki/File:Open_Access_logo_PLoS_white.svg art designer at PLoS, modified by Wikipedia users Nina, Beao, JakobVoss, and AnonMoos http://www.plos.org/
    Authors: Lembrechts, Jonas J; Van Den Hoogen, Johan; Aalto, Juha; Ashcroft, Michael B; +196 Authors

    AbstractResearch in global change ecology relies heavily on global climatic grids derived from estimates of air temperature in open areas at around 2 m above the ground. These climatic grids do not reflect conditions below vegetation canopies and near the ground surface, where critical ecosystem functions occur and most terrestrial species reside. Here, we provide global maps of soil temperature and bioclimatic variables at a 1‐km2resolution for 0–5 and 5–15 cm soil depth. These maps were created by calculating the difference (i.e. offset) between in situ soil temperature measurements, based on time series from over 1200 1‐km2pixels (summarized from 8519 unique temperature sensors) across all the world's major terrestrial biomes, and coarse‐grained air temperature estimates from ERA5‐Land (an atmospheric reanalysis by the European Centre for Medium‐Range Weather Forecasts). We show that mean annual soil temperature differs markedly from the corresponding gridded air temperature, by up to 10°C (mean = 3.0 ± 2.1°C), with substantial variation across biomes and seasons. Over the year, soils in cold and/or dry biomes are substantially warmer (+3.6 ± 2.3°C) than gridded air temperature, whereas soils in warm and humid environments are on average slightly cooler (−0.7 ± 2.3°C). The observed substantial and biome‐specific offsets emphasize that the projected impacts of climate and climate change on near‐surface biodiversity and ecosystem functioning are inaccurately assessed when air rather than soil temperature is used, especially in cold environments. The global soil‐related bioclimatic variables provided here are an important step forward for any application in ecology and related disciplines. Nevertheless, we highlight the need to fill remaining geographic gaps by collecting more in situ measurements of microclimate conditions to further enhance the spatiotemporal resolution of global soil temperature products for ecological applications.

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    image/svg+xml art designer at PLoS, modified by Wikipedia users Nina, Beao, JakobVoss, and AnonMoos Open Access logo, converted into svg, designed by PLoS. This version with transparent background. http://commons.wikimedia.org/wiki/File:Open_Access_logo_PLoS_white.svg art designer at PLoS, modified by Wikipedia users Nina, Beao, JakobVoss, and AnonMoos http://www.plos.org/
    image/svg+xml art designer at PLoS, modified by Wikipedia users Nina, Beao, JakobVoss, and AnonMoos Open Access logo, converted into svg, designed by PLoS. This version with transparent background. http://commons.wikimedia.org/wiki/File:Open_Access_logo_PLoS_white.svg art designer at PLoS, modified by Wikipedia users Nina, Beao, JakobVoss, and AnonMoos http://www.plos.org/
    image/svg+xml art designer at PLoS, modified by Wikipedia users Nina, Beao, JakobVoss, and AnonMoos Open Access logo, converted into svg, designed by PLoS. This version with transparent background. http://commons.wikimedia.org/wiki/File:Open_Access_logo_PLoS_white.svg art designer at PLoS, modified by Wikipedia users Nina, Beao, JakobVoss, and AnonMoos http://www.plos.org/
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    Global Change Biology
    Article . 2022 . Peer-reviewed
    License: CC BY NC
    Data sources: Crossref
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    Global Change Biology
    Article
    License: implied-oa
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    https://doi.org/10.32942/osf.i...
    Article . 2021 . Peer-reviewed
    License: CC BY SA
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    Research Collection
    Article . 2022
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    Data sources: Datacite
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    https://dx.doi.org/10.5445/ir/...
    Article . 2022
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    https://dx.doi.org/10.21256/zh...
    Article . 2022
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    ZENODO
    Article . 2022
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    Research Collection
    Article . 2022
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    Wageningen Staff Publications
    Article . 2022
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    Munin - Open Research Archive
    Article . 2021 . Peer-reviewed
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    Munin - Open Research Archive
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    Apollo
    Article . 2022
    Data sources: Datacite
    CNR ExploRA
    Article . 2022
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    Access Routes
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      Global Change Biology
      Article . 2022 . Peer-reviewed
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      Global Change Biology
      Article
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      https://doi.org/10.32942/osf.i...
      Article . 2021 . Peer-reviewed
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      Research Collection
      Article . 2022
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      Data sources: Datacite
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      https://dx.doi.org/10.5445/ir/...
      Article . 2022
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      https://dx.doi.org/10.21256/zh...
      Article . 2022
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      ZENODO
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      Research Collection
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      Wageningen Staff Publications
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      Munin - Open Research Archive
      Article . 2021 . Peer-reviewed
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      Munin - Open Research Archive
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      Apollo
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      CNR ExploRA
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      Data sources: CNR ExploRA
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    Authors: Mariana García Criado; Isla H. Myers-Smith; Anne D. Bjorkman; Signe Normand; +37 Authors

    Climate change is leading to a species redistributions. In the tundra biome, many shrub species are expanding into new areas, a process known as shrubification. However, not all tundra shrub species will benefit from warming. Winner and loser species (those projected to expand and contract their ranges, and/or those that have increased or decreased in cover over time), and the characteristics that may determine success or failure, have not been fully identified. Here, we investigate whether current range sizes are related to plant trait values and intraspecific trait variation by combining 17,921 trait records and distribution data from 62 shrub species across three continents (>30 degrees north). In addition, we determine which traits are associated with species projected by species distribution models to expand or contract their ranges under climate change, and species that have undergone past cover changes over time. Winner and loser shrub species identified from projected range shifts generally differed from those identified from observed past cover change. We found that greater variation in seed mass and specific leaf area were related to larger projected range shifts. Projected winner species generally had greater seed mass values than ‘no change’ and loser species. However, contrary to our expectations, traits’ values and variation were not consistently related to current and projected ranges, and depended upon the future climate scenarios considered in range projections. There were no clear relationships either between cover change over time and trait values or variation. Overall, our findings indicate that abundance changes and projected range shifts will not lead to directional modifications in shrub trait composition or variation with future warming, since winner and loser species share relatively similar trait spaces based on commonly measured traits. Future research could investigate other morpho-physiological traits underpinning climatic preferences, which might better predict future range and abundance changes.

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    Nature Communications
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    Nature Communications
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    https://doi.org/10.32942/x23s3...
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      Nature Communications
      Article . 2023 . Peer-reviewed
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      Nature Communications
      Article . 2023
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      https://doi.org/10.32942/x23s3...
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    Authors: Isla H. Myers‐Smith; Haydn J. D. Thomas; Anne D. Bjorkman;

    Contents Summary 1742 I. Introduction 1742 II. The global context of tundra trait variation 1743 III. The current state of knowledge on trait change in the tundra biome 1744 IV. The links between traits and ecosystem functions 1744 V. Future priorities for tundra trait research 1746 VI. Conclusions 1746 References 1747 SummaryIn the rapidly warming tundra biome, plant traits provide an essential link between ongoing vegetation change and feedbacks to key ecosystem functions. However, only recently have comprehensive trait data been compiled for tundra species and sites, allowing us to assess key elements of functional responses to global change. In this review, we summarize trait‐based research in tundra ecosystems, with a focus on three components: plant trait variation and how it compares with global patterns; shifts in community‐level traits in response to environmental change; and the use of traits to understand and predict ecosystem function. Quantifying patterns and trends in plant traits will allow us to better project the consequences of environmental change for the ecology and functioning of tundra ecosystems.

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    New Phytologist
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    New Phytologist
    Article . 2018 . Peer-reviewed
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      New Phytologist
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      Article . 2020
  • Authors: Dov F. Sax; Antoine Becker-Scarpitta; Jenny L. McCune; Isla H. Myers-Smith; +4 Authors

    Plant communities have undergone dramatic changes in recent centuries, although not all such changes fit with the dominant biodiversity-crisis narrative used to describe them. At the global scale, future declines in plant species diversity are highly likely given habitat conversion in the tropics, although few extinctions have been documented for the Anthropocene to date (<0.1%). Nonnative species introductions have greatly increased plant species richness in many regions of the world at the same time that they have led to the creation of new hybrid polyploid species by bringing previously isolated congeners into close contact. At the local scale, conversion of primary vegetation to agriculture has decreased plant diversity, whereas other drivers of change—e.g., climate warming, habitat fragmentation, and nitrogen deposition—have highly context-dependent effects, resulting in a distribution of temporal trends with a mean close to zero. These results prompt a reassessment of how conservation goals are defined and justified.

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    Authors: Logan T. Berner; Richard Massey; Patrick Jantz; Bruce C. Forbes; +10 Authors

    AbstractArctic warming can influence tundra ecosystem function with consequences for climate feedbacks, wildlife and human communities. Yet ecological change across the Arctic tundra biome remains poorly quantified due to field measurement limitations and reliance on coarse-resolution satellite data. Here, we assess decadal changes in Arctic tundra greenness using time series from the 30 m resolution Landsat satellites. From 1985 to 2016 tundra greenness increased (greening) at ~37.3% of sampling sites and decreased (browning) at ~4.7% of sampling sites. Greening occurred most often at warm sampling sites with increased summer air temperature, soil temperature, and soil moisture, while browning occurred most often at cold sampling sites that cooled and dried. Tundra greenness was positively correlated with graminoid, shrub, and ecosystem productivity measured at field sites. Our results support the hypothesis that summer warming stimulated plant productivity across much, but not all, of the Arctic tundra biome during recent decades.

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    Nature Communications
    Article . 2020 . Peer-reviewed
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    Nature Communications
    Article . 2020
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      Nature Communications
      Article . 2020
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    Authors: Jelte Rozema; Ken D. Tape; Niels Martin Schmidt; Susanna Venn; +29 Authors

    Abstract Recent research using repeat photography, long-term ecological monitoring and dendrochronology has documented shrub expansion in arctic, high-latitude and alpine tundra ecosystems. Here, we (1) synthesize these findings, (2) present a conceptual framework that identifies mechanisms and constraints on shrub increase, (3) explore causes, feedbacks and implications of the increased shrub cover in tundra ecosystems, and (4) address potential lines of investigation for future research. Satellite observations from around the circumpolar Arctic, showing increased productivity, measured as changes in ‘greenness’, have coincided with a general rise in high-latitude air temperatures and have been partly attributed to increases in shrub cover. Studies indicate that warming temperatures, changes in snow cover, altered disturbance regimes as a result of permafrost thaw, tundra fires, and anthropogenic activities or changes in herbivory intensity are all contributing to observed changes in shrub abundance. A large-scale increase in shrub cover will change the structure of tundra ecosystems and alter energy fluxes, regional climate, soil–atmosphere exchange of water, carbon and nutrients, and ecological interactions between species. In order to project future rates of shrub expansion and understand the feedbacks to ecosystem and climate processes, future research should investigate the species or trait-specific responses of shrubs to climate change including: (1) the temperature sensitivity of shrub growth, (2) factors controlling the recruitment of new individuals, and (3) the relative influence of the positive and negative feedbacks involved in shrub expansion.

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    Environmental Research Letters
    Article . 2011 . Peer-reviewed
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    Environmental Research Letters
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    Munin - Open Research Archive
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      Article . 2011 . Peer-reviewed
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    Authors: Mark Vellend; Carissa D. Brown; Heather M. Kharouba; Isla H. Myers-Smith; +1 Authors

    Predicting the future ecological impact of global change drivers requires understanding how these same drivers have acted in the past to produce the plant populations and communities we see today. Historical ecological data sources have made contributions of central importance to global change biology, but remain outside the toolkit of most ecologists. Here we review the strengths and weaknesses of four unconventional sources of historical ecological data: land survey records, “legacy” vegetation data, historical maps and photographs, and herbarium specimens. We discuss recent contributions made using these data sources to understanding the impacts of habitat disturbance and climate change on plant populations and communities, and the duration of extinction–colonization time lags in response to landscape change. Historical data frequently support inferences made using conventional ecological studies (e.g., increases in warm‐adapted species as temperature rises), but there are cases when the addition of different data sources leads to different conclusions (e.g., temporal vegetation change not as predicted by chronosequence studies). The explicit combination of historical and contemporary data sources is an especially powerful approach for unraveling long‐term consequences of multiple drivers of global change. Despite the limitations of historical data, which include spotty and potentially biased spatial and temporal coverage, they often represent the only means of characterizing ecological phenomena in the past and have proven indispensable for characterizing the nature, magnitude, and generality of global change impacts on plant populations and communities.

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    American Journal of Botany
    Article . 2013 . Peer-reviewed
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      American Journal of Botany
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  • Authors: Daskalova, Gergana; Myers-Smith, Isla; Bowler, Diana; Dornelas, Maria; +7 Authors

    Our aim is to quantify how global change drivers influence species’ populations and biodiversity change. Specifically, we will focus on the effects of climate change, human use, human population density, pollution and invasion pressure on temporal changes in population abundance, species richness and community composition (turnover), as these drivers capture the variety of ways in which humans are altering the planet. We will test if the individual, cumulative and interactive effects of the different types of global change explain the heterogeneous patterns of population and biodiversity change observed across the planet.

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    Authors: Callaghan, Terry V.; Tweedie, Craig E.; Åkerman, Jonas; Andrews, Christopher; +49 Authors

    Understanding the responses of tundra systems to global change has global implications. Most tundra regions lack sustained environmental monitoring and one of the only ways to document multi-decadal change is to resample historic research sites. The International Polar Year (IPY) provided a unique opportunity for such research through the Back to the Future (BTF) project (IPY project #512). This article synthesizes the results from 13 papers within this Ambio Special Issue. Abiotic changes include glacial recession in the Altai Mountains, Russia; increased snow depth and hardness, permafrost warming, and increased growing season length in sub-arctic Sweden; drying of ponds in Greenland; increased nutrient availability in Alaskan tundra ponds, and warming at most locations studied. Biotic changes ranged from relatively minor plant community change at two sites in Greenland to moderate change in the Yukon, and to dramatic increases in shrub and tree density on Herschel Island, and in subarctic Sweden. The population of geese tripled at one site in northeast Greenland where biomass in non-grazed plots doubled. A model parameterized using results from a BTF study forecasts substantial declines in all snowbeds and increases in shrub tundra on Niwot Ridge, Colorado over the next century. In general, results support and provide improved capacities for validating experimental manipulation, remote sensing, and modeling studies.

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    AMBIO
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    DSpace at VU
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    AMBIO
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    Research at ASB
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    AMBIO
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    Authors: Daskalova, Gergana N.; Myers-Smith, Isla H.; Godlee, John L.;

    AbstractThe Earth’s biota is changing over time in complex ways. A critical challenge is to test whether specific biomes, taxa or types of species benefit or suffer in a time of accelerating global change. We analysed nearly 10,000 abundance time series from over 2000 vertebrate species part of the Living Planet Database. We integrated abundance data with information on geographic range, habitat preference, taxonomic and phylogenetic relationships, and IUCN Red List Categories and threats. We find that 15% of populations declined, 18% increased, and 67% showed no net changes over time. Against a backdrop of no biogeographic and phylogenetic patterning in population change, we uncover a distinct taxonomic signal. Amphibians were the only taxa that experienced net declines in the analysed data, while birds, mammals and reptiles experienced net increases. Population trends were poorly captured by species’ rarity and global-scale threats. Incorporation of the full spectrum of population change will improve conservation efforts to protect global biodiversity.

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