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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: Robert Rauschkolb; Solveig Franziska Bucher; Isabell Hensen; Antje Ahrends; +30 Authors

    Abstract Whereas temporal variability of plant phenology in response to climate change has already been well studied, the spatial variability of phenology is not well understood. Given that phenological shifts may affect the magnitude of biotic interactions, there is a need to investigate how the variability in environmental factors relates to the spatial variability in herbaceous species’ phenology by at the same time considering their functional traits to predict their general and species-specific responses to future climate change. In this project, we analysed phenology records of 148 herbaceous species, which were observed for a single year by the PhenObs network in 15 botanical gardens. For each species, we characterised the spatial variability in six different phenological stages across gardens. We used boosted regression trees to link these variabilities in phenology to the variability in environmental parameters (temperature, latitude, and local habitat conditions) as well as species traits (seed mass, vegetative height, specific leaf area, and temporal niche) hypothesised to be related to phenology variability. We found that spatial variability in the phenology of herbaceous species was mainly driven by the variability in temperature but also photoperiod was an important driving factor for some phenological stages. In addition, we found that early-flowering and less competitive species indicated by small specific leaf area and vegetative height were more variable in their phenology. Our findings contribute to the field of phenology by showing that besides temperature, photoperiod and functional traits are important to be included when spatial variability of herbaceous species is investigated.

    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/10.2...arrow_drop_down
    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/10.21203/rs.3....
    Article . 2023 . Peer-reviewed
    License: CC BY
    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/
    International Journal of Biometeorology
    Article . 2024 . Peer-reviewed
    License: CC BY
    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/
    https://dx.doi.org/10.17169/re...
    Other literature type . 2024
    License: CC BY
    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/
    PubMed Central
    Other literature type . 2024
    License: CC BY
    Data sources: PubMed Central
    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/
    DIGITAL.CSIC
    Article . 2024 . Peer-reviewed
    Data sources: DIGITAL.CSIC
    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/
    addClaim

    This Research product is the result of merged Research products in OpenAIRE.

    You have already added works in your ORCID record related to the merged Research product.
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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/ https://doi.org/10.2...arrow_drop_down
      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/10.21203/rs.3....
      Article . 2023 . Peer-reviewed
      License: CC BY
      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/
      International Journal of Biometeorology
      Article . 2024 . Peer-reviewed
      License: CC BY
      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/
      https://dx.doi.org/10.17169/re...
      Other literature type . 2024
      License: CC BY
      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/
      PubMed Central
      Other literature type . 2024
      License: CC BY
      Data sources: PubMed Central
      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/
      DIGITAL.CSIC
      Article . 2024 . Peer-reviewed
      Data sources: DIGITAL.CSIC
      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/
      addClaim

      This Research product is the result of merged Research products in OpenAIRE.

      You have already added works in your ORCID record related to the merged Research product.
  • 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: Robert Rauschkolb; Solveig Franziska Bucher; Isabell Hensen; Antje Ahrends; +30 Authors

    Abstract Whereas temporal variability of plant phenology in response to climate change has already been well studied, the spatial variability of phenology is not well understood. Given that phenological shifts may affect the magnitude of biotic interactions, there is a need to investigate how the variability in environmental factors relates to the spatial variability in herbaceous species’ phenology by at the same time considering their functional traits to predict their general and species-specific responses to future climate change. In this project, we analysed phenology records of 148 herbaceous species, which were observed for a single year by the PhenObs network in 15 botanical gardens. For each species, we characterised the spatial variability in six different phenological stages across gardens. We used boosted regression trees to link these variabilities in phenology to the variability in environmental parameters (temperature, latitude, and local habitat conditions) as well as species traits (seed mass, vegetative height, specific leaf area, and temporal niche) hypothesised to be related to phenology variability. We found that spatial variability in the phenology of herbaceous species was mainly driven by the variability in temperature but also photoperiod was an important driving factor for some phenological stages. In addition, we found that early-flowering and less competitive species indicated by small specific leaf area and vegetative height were more variable in their phenology. Our findings contribute to the field of phenology by showing that besides temperature, photoperiod and functional traits are important to be included when spatial variability of herbaceous species is investigated.

    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/10.2...arrow_drop_down
    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/10.21203/rs.3....
    Article . 2023 . Peer-reviewed
    License: CC BY
    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/
    International Journal of Biometeorology
    Article . 2024 . Peer-reviewed
    License: CC BY
    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/
    https://dx.doi.org/10.17169/re...
    Other literature type . 2024
    License: CC BY
    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/
    PubMed Central
    Other literature type . 2024
    License: CC BY
    Data sources: PubMed Central
    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/
    DIGITAL.CSIC
    Article . 2024 . Peer-reviewed
    Data sources: DIGITAL.CSIC
    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/
    addClaim

    This Research product is the result of merged Research products in OpenAIRE.

    You have already added works in your ORCID record related to the merged Research product.
    5
    citations5
    popularityAverage
    influenceAverage
    impulseTop 10%
    BIP!Powered by BIP!
    more_vert
      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/10.2...arrow_drop_down
      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/10.21203/rs.3....
      Article . 2023 . Peer-reviewed
      License: CC BY
      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/
      International Journal of Biometeorology
      Article . 2024 . Peer-reviewed
      License: CC BY
      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/
      https://dx.doi.org/10.17169/re...
      Other literature type . 2024
      License: CC BY
      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/
      PubMed Central
      Other literature type . 2024
      License: CC BY
      Data sources: PubMed Central
      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/
      DIGITAL.CSIC
      Article . 2024 . Peer-reviewed
      Data sources: DIGITAL.CSIC
      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/
      addClaim

      This Research product is the result of merged Research products in OpenAIRE.

      You have already added works in your ORCID record related to the merged Research product.
  • 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: Ulisse Gomarasca; Mirco Migliavacca; Jens Kattge; Jacob A. Nelson; +40 Authors

    AbstractFundamental axes of variation in plant traits result from trade-offs between costs and benefits of resource-use strategies at the leaf scale. However, it is unclear whether similar trade-offs propagate to the ecosystem level. Here, we test whether trait correlation patterns predicted by three well-known leaf- and plant-level coordination theories – the leaf economics spectrum, the global spectrum of plant form and function, and the least-cost hypothesis – are also observed between community mean traits and ecosystem processes. We combined ecosystem functional properties from FLUXNET sites, vegetation properties, and community mean plant traits into three corresponding principal component analyses. We find that the leaf economics spectrum (90 sites), the global spectrum of plant form and function (89 sites), and the least-cost hypothesis (82 sites) all propagate at the ecosystem level. However, we also find evidence of additional scale-emergent properties. Evaluating the coordination of ecosystem functional properties may aid the development of more realistic global dynamic vegetation models with critical empirical data, reducing the uncertainty of climate change projections.

    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/ IRIS Cnrarrow_drop_down
    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/
    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/
    Nature Communications
    Article . 2023 . Peer-reviewed
    License: CC BY
    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/
    https://doi.org/10.21203/rs.3....
    Article . 2023 . Peer-reviewed
    License: CC BY
    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/
    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/
    CNR ExploRA
    Article . 2023
    Data sources: CNR ExploRA
    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/
    Nature Communications
    Article . 2023
    Data sources: DOAJ
    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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    HAL INRAE
    Article . 2023
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    Article . 2023
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    Nature Communications
    Article . 2023 . Peer-reviewed
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    Article . 2023
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    Authors: Ulisse Gomarasca; Mirco Migliavacca; Jens Kattge; Jacob A. Nelson; +40 Authors

    AbstractFundamental axes of variation in plant traits result from trade-offs between costs and benefits of resource-use strategies at the leaf scale. However, it is unclear whether similar trade-offs propagate to the ecosystem level. Here, we test whether trait correlation patterns predicted by three well-known leaf- and plant-level coordination theories – the leaf economics spectrum, the global spectrum of plant form and function, and the least-cost hypothesis – are also observed between community mean traits and ecosystem processes. We combined ecosystem functional properties from FLUXNET sites, vegetation properties, and community mean plant traits into three corresponding principal component analyses. We find that the leaf economics spectrum (90 sites), the global spectrum of plant form and function (89 sites), and the least-cost hypothesis (82 sites) all propagate at the ecosystem level. However, we also find evidence of additional scale-emergent properties. Evaluating the coordination of ecosystem functional properties may aid the development of more realistic global dynamic vegetation models with critical empirical data, reducing the uncertainty of climate change projections.

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    Nature Communications
    Article . 2023 . Peer-reviewed
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    https://doi.org/10.21203/rs.3....
    Article . 2023 . Peer-reviewed
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    Article . 2023
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    Article . 2023
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    Nature Communications
    Article . 2023 . Peer-reviewed
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    Article . 2023
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    Authors: Simone Cesarz; Nico Eisenhauer; Solveig Franziska Bucher; Marcel Ciobanu; +1 Authors

    Artificial light at night (ALAN) is increasing worldwide, but its effects on the soil system have not yet been investigated. We tested the influence of experimental manipulation of ALAN on two taxa of soil communities (microorganisms and soil nematodes) and three aspects of soil functioning (soil basal respiration, soil microbial biomass and carbon use efficiency) over four and a half months in a highly controlled Ecotron facility. We show that during peak plant biomass, increasing ALAN reduced plant biomass and was also associated with decreased soil water content. This further reduced soil respiration under high ALAN at peak plant biomass, but microbial communities maintained stable biomass across different levels of ALAN and times, demonstrating higher microbial carbon use efficiency under high ALAN. While ALAN did not affect microbial community structure, the abundance of plant-feeding nematodes increased and there was homogenization of nematode communities under higher levels of ALAN, indicating that soil communities may be more vulnerable to additional disturbances at high ALAN. In summary, the effects of ALAN reach into the soil system by altering soil communities and ecosystem functions, and these effects are mediated by changes in plant productivity and soil water content at peak plant biomass. This article is part of the theme issue ‘Light pollution in complex ecological systems’.

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    Philosophical Transactions of the Royal Society B Biological Sciences
    Article . 2023 . Peer-reviewed
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    Authors: Simone Cesarz; Nico Eisenhauer; Solveig Franziska Bucher; Marcel Ciobanu; +1 Authors

    Artificial light at night (ALAN) is increasing worldwide, but its effects on the soil system have not yet been investigated. We tested the influence of experimental manipulation of ALAN on two taxa of soil communities (microorganisms and soil nematodes) and three aspects of soil functioning (soil basal respiration, soil microbial biomass and carbon use efficiency) over four and a half months in a highly controlled Ecotron facility. We show that during peak plant biomass, increasing ALAN reduced plant biomass and was also associated with decreased soil water content. This further reduced soil respiration under high ALAN at peak plant biomass, but microbial communities maintained stable biomass across different levels of ALAN and times, demonstrating higher microbial carbon use efficiency under high ALAN. While ALAN did not affect microbial community structure, the abundance of plant-feeding nematodes increased and there was homogenization of nematode communities under higher levels of ALAN, indicating that soil communities may be more vulnerable to additional disturbances at high ALAN. In summary, the effects of ALAN reach into the soil system by altering soil communities and ecosystem functions, and these effects are mediated by changes in plant productivity and soil water content at peak plant biomass. This article is part of the theme issue ‘Light pollution in complex ecological systems’.

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    Philosophical Transactions of the Royal Society B Biological Sciences
    Article . 2023 . Peer-reviewed
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    Authors: Bucher, Solveig Franziska; Uhde, Lia; Weigelt, Alexandra; Cesarz, Simone; +5 Authors

    The EcoUnits were filled with 1.23 m3 of unsterilised, well-mixed soil from the vicinity of the EcoTron, as we also monitored soil communities in the same experimental setup (see Cesarz et al.). Plant communities comprising 16 plant species were sown into soil on 19 February 2020 (see Table S1). Because the soil was not sterilised, some of the local seed bank was also transferred into our experiment. Plant communities were harvested by clipping aboveground plant biomass (2 cm above topsoil) on June 11, July 3, and August 28 (establishment period), as well as on October 27 and December 8 (measurement period). This harvest regime mimics typical intensive grassland management in central Europe, with short growth phases in between harvest events. For this study, we analysed the last two harvests in detail to address temporal variations and accumulated effects of the ALAN treatment (see Table S1; hereafter referred to harvest 1 and 2, respectively). The harvests differed in length: harvest 1 encompassed a time for regrowth of 9 weeks, whereas harvest 2 only encompassed 6 weeks, as this was embedded in a bigger experimental setup. The biomass of one-eighth (0.19 m2) of each EcoUnit (subplot) was separated into species (both sown and not sown as well as ‘unknown’) and then dried to constant weight at 60°C for three days. Plant identification was sometimes not possible when the plants were not fully mature. These species were all clustered as ‘unknown species’, whereas for others only the genus could be determined. Dead biomass was also recorded. Plant functional trait data was collected for one species each per functional group of grasses (B. hordeaceus), non-legume forbs (P. lanceolata) and legumes (T. repens) just before the harvests in October and December. The species were selected based on their frequent occurrence in the EcoUnits. However, not all plant traits were measured on all species and in all EcoUnits. P. lanceolata was originally not sown into the communities but had become one of the dominant species in the EcoUnits by October and was thus selected for our experiment. It was not very abundant by the end of the experiment as it did not regenerate well after the harvest in October. All traits were collected and measured just before the harvest unless stated otherwise. Stretched plant height of three representative individuals per species and EcoUnit was measured using a ruler. Then, ten healthy leaves from at least three manually randomly selected individuals per species and EcoUnit were harvested and transported to the laboratory, where SLA, LDMC, toughness, hairiness and wettability were measured. All ten leaves were scanned on an Epson Expression 11000 XL scanner and the resulting images were analysed using ImageJ to determine the leaf area. In the case of T. repens, only the lamina was scanned. Leaves were weighed and subsequently dried at 70°C for at least 48h, and dry weight was recorded to calculate SLA (leaf area of fresh leaf/ dry weight) and LDMC (dry weight/ fresh weight). All weights were measured using a precision scale (QUINTIX315_1S, Sartorius Lab Instruments GmbH & Co. KG, Goettingen, Germany). A few days afterwards, the chlorophyll fluorescence measurements and the SPAD values were determined on living plants in the EcoUnits, just before the harvests. The hairiness, or rather the density of trichomes, of the leaves was analysed by counting the hairs from an image taken at 400-fold magnification using a light microscope and focussing on the middle part of the leaf (Ocular 10x/22, Di-Li-2009, Distelkamp-Electronic, Kaiserslautern, Germany) in ImageJ. For that, four of the leaves used in SLA measurements were chosen at random. Hairs were counted on the upper and lower leaf side and then added to make a total for both leaf sites. T. repens did not show any hair on its lamina. The samples of this species were excluded from the subsequent analysis. The leaf thickness was measured with a digital caliper (WEZU Messwerkzeuge Remscheid GmbH, Remscheid, Germany) at the same spot as leaf toughness. For leaf toughness, the puncture resistance was measured using a surgical blade at a speed of 129 mm min-1 on an electric test stand (Sauter GmbH, Wutöschingen, Germany) and the force of the cut was measured with a power meter (FH 50, Sauter GmbH). The leaf toughness was than calculated as the quotient between the puncture resistance and the thickness. The leaf wettability was investigated via measuring the contact angle (CA) of a water droplet and the leaf, where high CA means low wettability. For that, a droplet of 5 µl distilled water was placed on a flat leaf surface for 90 seconds and then photographed (Nikon D5300 with a Sigma DC Objective, Chiyoda, Tokyo, Japan). The CA was then measured using ImageJ. Chlorophyll fluorescence was measured using a PocketPEA device (Hansatech, King’s Lynn, Norfolk, UK). We measured the parameters PIabs as well as plant stress via Fv/Fm after 30 min of dark adaption to ensure a full reduction of the photosystems on three replicate individuals for each EcoUnit and species. These measurements were not performed on P. lanceolata, as not many individuals were abundant after harvesting the leaves for the previous analysis. The SPAD value was measured using a SPAD 502 (Minolta Camera Co., Osaka, Japan) on the same individual. For each individual, three replicate measurements were performed as the values varied within individuals. # Artificial light at night (ALAN) decreases plant diversity and performance in experimental grassland communities – Data on species biomass and traits [https://doi.org/10.5061/dryad.hhmgqnknt](https://doi.org/10.5061/dryad.hhmgqnknt) In ALAN\_specis\_biomass.csv, Biomass per species in the proportion sorted is given. In ALAN\_biomass.csv, the biomass of the entire Ecotron is given. In ALAN\_traits.csv, traits of the species are given. ## Description of the data and file structure ALAN\_specis\_biomass.csv: The species are abbreviated by 3 letters genus and species. unit describes the name of the EcoUnit (numbered consecutively), light refers to the light regime (given in lux), mass indicates the biomass (in g dry matter) and harvest denotes whether it was the first or 2nd harvest studied (categorical information). ALAN\_biomass.csv: biomass refers to biomass (g dry matter), unit describes the name of the EcoUnit (numbered consecutively), and harvest denotes whether it was the first or 2nd harvest studied. Treatment refers to the light regime (in lux). ALAN\_traits.csv: Species and EcoUnit are given as above. Treatment refers to the light regime (in lux).. Hair density is hairiness (hairs mm-2), besides that toughness (N mm-1), contact angle (CA\_Mean, °), fresh weight (g), dry weight (g), leaf area (cm2), specific leaf area (SLA; cm2 g-1), leaf dry matter content (mg g-1), SPAD, plant height (cm) and the chlorophyll parameters FvFm and PIabs are given as described in Methods. Artificial light at night (ALAN) affects many areas of the world and is increasing globally. To date, there has been limited and inconsistent evidence regarding the consequences of ALAN on plant communities as well as the fitness of their constituent species. ALAN could be beneficial for plants as they need light as an energy source, but they also need darkness for regeneration and growth. We created model communities composed of 16 plant species sown, exposed to a gradient of ALAN ranging from ‘moonlight only’ to conditions like situations typically found directly underneath a streetlamp. We measured plant community composition and its production (biomass), as well as functional traits of three plant species from different functional groups (grasses, herbs, legumes) in two separate harvests. We found that biomass was reduced by 33% in the highest ALAN treatment compared to the control, Shannon diversity decreased by 43% and Evenness by 34% in the first harvest. Some species failed to establish in the second harvest. Specific leaf area, leaf dry matter content and leaf hairiness responded to ALAN. These responses suggest that plant communities will be sensitive to increasing ALAN, and they flag a need for plant conservation activities that consider impending ALAN scenarios.

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    ZENODO
    Dataset . 2023
    License: CC 0
    Data sources: ZENODO
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    ZENODO
    Dataset . 2023
    License: CC 0
    Data sources: ZENODO
    DRYAD
    Dataset . 2023
    License: CC 0
    Data sources: Datacite
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      ZENODO
      Dataset . 2023
      License: CC 0
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      Dataset . 2023
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    Authors: Bucher, Solveig Franziska; Uhde, Lia; Weigelt, Alexandra; Cesarz, Simone; +5 Authors

    The EcoUnits were filled with 1.23 m3 of unsterilised, well-mixed soil from the vicinity of the EcoTron, as we also monitored soil communities in the same experimental setup (see Cesarz et al.). Plant communities comprising 16 plant species were sown into soil on 19 February 2020 (see Table S1). Because the soil was not sterilised, some of the local seed bank was also transferred into our experiment. Plant communities were harvested by clipping aboveground plant biomass (2 cm above topsoil) on June 11, July 3, and August 28 (establishment period), as well as on October 27 and December 8 (measurement period). This harvest regime mimics typical intensive grassland management in central Europe, with short growth phases in between harvest events. For this study, we analysed the last two harvests in detail to address temporal variations and accumulated effects of the ALAN treatment (see Table S1; hereafter referred to harvest 1 and 2, respectively). The harvests differed in length: harvest 1 encompassed a time for regrowth of 9 weeks, whereas harvest 2 only encompassed 6 weeks, as this was embedded in a bigger experimental setup. The biomass of one-eighth (0.19 m2) of each EcoUnit (subplot) was separated into species (both sown and not sown as well as ‘unknown’) and then dried to constant weight at 60°C for three days. Plant identification was sometimes not possible when the plants were not fully mature. These species were all clustered as ‘unknown species’, whereas for others only the genus could be determined. Dead biomass was also recorded. Plant functional trait data was collected for one species each per functional group of grasses (B. hordeaceus), non-legume forbs (P. lanceolata) and legumes (T. repens) just before the harvests in October and December. The species were selected based on their frequent occurrence in the EcoUnits. However, not all plant traits were measured on all species and in all EcoUnits. P. lanceolata was originally not sown into the communities but had become one of the dominant species in the EcoUnits by October and was thus selected for our experiment. It was not very abundant by the end of the experiment as it did not regenerate well after the harvest in October. All traits were collected and measured just before the harvest unless stated otherwise. Stretched plant height of three representative individuals per species and EcoUnit was measured using a ruler. Then, ten healthy leaves from at least three manually randomly selected individuals per species and EcoUnit were harvested and transported to the laboratory, where SLA, LDMC, toughness, hairiness and wettability were measured. All ten leaves were scanned on an Epson Expression 11000 XL scanner and the resulting images were analysed using ImageJ to determine the leaf area. In the case of T. repens, only the lamina was scanned. Leaves were weighed and subsequently dried at 70°C for at least 48h, and dry weight was recorded to calculate SLA (leaf area of fresh leaf/ dry weight) and LDMC (dry weight/ fresh weight). All weights were measured using a precision scale (QUINTIX315_1S, Sartorius Lab Instruments GmbH & Co. KG, Goettingen, Germany). A few days afterwards, the chlorophyll fluorescence measurements and the SPAD values were determined on living plants in the EcoUnits, just before the harvests. The hairiness, or rather the density of trichomes, of the leaves was analysed by counting the hairs from an image taken at 400-fold magnification using a light microscope and focussing on the middle part of the leaf (Ocular 10x/22, Di-Li-2009, Distelkamp-Electronic, Kaiserslautern, Germany) in ImageJ. For that, four of the leaves used in SLA measurements were chosen at random. Hairs were counted on the upper and lower leaf side and then added to make a total for both leaf sites. T. repens did not show any hair on its lamina. The samples of this species were excluded from the subsequent analysis. The leaf thickness was measured with a digital caliper (WEZU Messwerkzeuge Remscheid GmbH, Remscheid, Germany) at the same spot as leaf toughness. For leaf toughness, the puncture resistance was measured using a surgical blade at a speed of 129 mm min-1 on an electric test stand (Sauter GmbH, Wutöschingen, Germany) and the force of the cut was measured with a power meter (FH 50, Sauter GmbH). The leaf toughness was than calculated as the quotient between the puncture resistance and the thickness. The leaf wettability was investigated via measuring the contact angle (CA) of a water droplet and the leaf, where high CA means low wettability. For that, a droplet of 5 µl distilled water was placed on a flat leaf surface for 90 seconds and then photographed (Nikon D5300 with a Sigma DC Objective, Chiyoda, Tokyo, Japan). The CA was then measured using ImageJ. Chlorophyll fluorescence was measured using a PocketPEA device (Hansatech, King’s Lynn, Norfolk, UK). We measured the parameters PIabs as well as plant stress via Fv/Fm after 30 min of dark adaption to ensure a full reduction of the photosystems on three replicate individuals for each EcoUnit and species. These measurements were not performed on P. lanceolata, as not many individuals were abundant after harvesting the leaves for the previous analysis. The SPAD value was measured using a SPAD 502 (Minolta Camera Co., Osaka, Japan) on the same individual. For each individual, three replicate measurements were performed as the values varied within individuals. # Artificial light at night (ALAN) decreases plant diversity and performance in experimental grassland communities – Data on species biomass and traits [https://doi.org/10.5061/dryad.hhmgqnknt](https://doi.org/10.5061/dryad.hhmgqnknt) In ALAN\_specis\_biomass.csv, Biomass per species in the proportion sorted is given. In ALAN\_biomass.csv, the biomass of the entire Ecotron is given. In ALAN\_traits.csv, traits of the species are given. ## Description of the data and file structure ALAN\_specis\_biomass.csv: The species are abbreviated by 3 letters genus and species. unit describes the name of the EcoUnit (numbered consecutively), light refers to the light regime (given in lux), mass indicates the biomass (in g dry matter) and harvest denotes whether it was the first or 2nd harvest studied (categorical information). ALAN\_biomass.csv: biomass refers to biomass (g dry matter), unit describes the name of the EcoUnit (numbered consecutively), and harvest denotes whether it was the first or 2nd harvest studied. Treatment refers to the light regime (in lux). ALAN\_traits.csv: Species and EcoUnit are given as above. Treatment refers to the light regime (in lux).. Hair density is hairiness (hairs mm-2), besides that toughness (N mm-1), contact angle (CA\_Mean, °), fresh weight (g), dry weight (g), leaf area (cm2), specific leaf area (SLA; cm2 g-1), leaf dry matter content (mg g-1), SPAD, plant height (cm) and the chlorophyll parameters FvFm and PIabs are given as described in Methods. Artificial light at night (ALAN) affects many areas of the world and is increasing globally. To date, there has been limited and inconsistent evidence regarding the consequences of ALAN on plant communities as well as the fitness of their constituent species. ALAN could be beneficial for plants as they need light as an energy source, but they also need darkness for regeneration and growth. We created model communities composed of 16 plant species sown, exposed to a gradient of ALAN ranging from ‘moonlight only’ to conditions like situations typically found directly underneath a streetlamp. We measured plant community composition and its production (biomass), as well as functional traits of three plant species from different functional groups (grasses, herbs, legumes) in two separate harvests. We found that biomass was reduced by 33% in the highest ALAN treatment compared to the control, Shannon diversity decreased by 43% and Evenness by 34% in the first harvest. Some species failed to establish in the second harvest. Specific leaf area, leaf dry matter content and leaf hairiness responded to ALAN. These responses suggest that plant communities will be sensitive to increasing ALAN, and they flag a need for plant conservation activities that consider impending ALAN scenarios.

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    ZENODO
    Dataset . 2023
    License: CC 0
    Data sources: ZENODO
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    ZENODO
    Dataset . 2023
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    DRYAD
    Dataset . 2023
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      ZENODO
      Dataset . 2023
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      ZENODO
      Dataset . 2023
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    Authors: Maria Sporbert; Desiree Jakubka; Solveig Franziska Bucher; Isabell Hensen; +19 Authors

    Summary Phenology has emerged as key indicator of the biological impacts of climate change, yet the role of functional traits constraining variation in herbaceous species’ phenology has received little attention. Botanical gardens are ideal places in which to investigate large numbers of species growing under common climate conditions. We ask whether interspecific variation in plant phenology is influenced by differences in functional traits. We recorded onset, end, duration and intensity of initial growth, leafing out, leaf senescence, flowering and fruiting for 212 species across five botanical gardens in Germany. We measured functional traits, including plant height, absolute and specific leaf area, leaf dry matter content, leaf carbon and nitrogen content and seed mass and accounted for species’ relatedness. Closely related species showed greater similarities in timing of phenological events than expected by chance, but species' traits had a high degree of explanatory power, pointing to paramount importance of species’ life‐history strategies. Taller plants showed later timing of initial growth, and flowered, fruited and underwent leaf senescence later. Large‐leaved species had shorter flowering and fruiting durations. Taller, large‐leaved species differ in their phenology and are more competitive than smaller, small‐leaved species. We assume climate warming will change plant communities’ competitive hierarchies with consequences for biodiversity.

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    New Phytologist
    Article . 2022 . Peer-reviewed
    License: CC BY
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    https://dx.doi.org/10.17169/re...
    Other literature type . 2022
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    Article . 2022
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    New Phytologist
    Article . 2022
    New Phytologist
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    Authors: Maria Sporbert; Desiree Jakubka; Solveig Franziska Bucher; Isabell Hensen; +19 Authors

    Summary Phenology has emerged as key indicator of the biological impacts of climate change, yet the role of functional traits constraining variation in herbaceous species’ phenology has received little attention. Botanical gardens are ideal places in which to investigate large numbers of species growing under common climate conditions. We ask whether interspecific variation in plant phenology is influenced by differences in functional traits. We recorded onset, end, duration and intensity of initial growth, leafing out, leaf senescence, flowering and fruiting for 212 species across five botanical gardens in Germany. We measured functional traits, including plant height, absolute and specific leaf area, leaf dry matter content, leaf carbon and nitrogen content and seed mass and accounted for species’ relatedness. Closely related species showed greater similarities in timing of phenological events than expected by chance, but species' traits had a high degree of explanatory power, pointing to paramount importance of species’ life‐history strategies. Taller plants showed later timing of initial growth, and flowered, fruited and underwent leaf senescence later. Large‐leaved species had shorter flowering and fruiting durations. Taller, large‐leaved species differ in their phenology and are more competitive than smaller, small‐leaved species. We assume climate warming will change plant communities’ competitive hierarchies with consequences for biodiversity.

    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/ New Phytologistarrow_drop_down
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    New Phytologist
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    https://dx.doi.org/10.17169/re...
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    Authors: Solveig Franziska Bucher; Lia Uhde; Alexandra Weigelt; Simone Cesarz; +6 Authors

    Artificial light at night (ALAN) affects many areas of the world and is increasing globally. To date, there has been limited and inconsistent evidence regarding the consequences of ALAN for plant communities, as well as for the fitness of their constituent species. ALAN could be beneficial for plants as they need light as energy source, but they also need darkness for regeneration and growth. We created model communities composed of 16 plant species sown, exposed to a gradient of ALAN ranging from ‘moonlight only’ to conditions like situations typically found directly underneath a streetlamp. We measured plant community composition and its production (biomass), as well as functional traits of three plant species from different functional groups (grasses, herbs, legumes) in two separate harvests. We found that biomass was reduced by 33% in the highest ALAN treatment compared to the control, Shannon diversity decreased by 43% and evenness by 34% in the first harvest. Some species failed to establish in the second harvest. Specific leaf area, leaf dry matter content and leaf hairiness responded to ALAN. These responses suggest that plant communities will be sensitive to increasing ALAN, and they flag a need for plant conservation activities that consider impending ALAN scenarios.This article is part of the theme issue ‘Light pollution in complex ecological systems’.

    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/ Philosophical Transa...arrow_drop_down
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    Philosophical Transactions of the Royal Society B Biological Sciences
    Article . 2023 . Peer-reviewed
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    Authors: Solveig Franziska Bucher; Lia Uhde; Alexandra Weigelt; Simone Cesarz; +6 Authors

    Artificial light at night (ALAN) affects many areas of the world and is increasing globally. To date, there has been limited and inconsistent evidence regarding the consequences of ALAN for plant communities, as well as for the fitness of their constituent species. ALAN could be beneficial for plants as they need light as energy source, but they also need darkness for regeneration and growth. We created model communities composed of 16 plant species sown, exposed to a gradient of ALAN ranging from ‘moonlight only’ to conditions like situations typically found directly underneath a streetlamp. We measured plant community composition and its production (biomass), as well as functional traits of three plant species from different functional groups (grasses, herbs, legumes) in two separate harvests. We found that biomass was reduced by 33% in the highest ALAN treatment compared to the control, Shannon diversity decreased by 43% and evenness by 34% in the first harvest. Some species failed to establish in the second harvest. Specific leaf area, leaf dry matter content and leaf hairiness responded to ALAN. These responses suggest that plant communities will be sensitive to increasing ALAN, and they flag a need for plant conservation activities that consider impending ALAN scenarios.This article is part of the theme issue ‘Light pollution in complex ecological systems’.

    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/ Philosophical Transa...arrow_drop_down
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    Philosophical Transactions of the Royal Society B Biological Sciences
    Article . 2023 . Peer-reviewed
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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: Robert Rauschkolb; Solveig Franziska Bucher; Isabell Hensen; Antje Ahrends; +30 Authors

    Abstract Whereas temporal variability of plant phenology in response to climate change has already been well studied, the spatial variability of phenology is not well understood. Given that phenological shifts may affect the magnitude of biotic interactions, there is a need to investigate how the variability in environmental factors relates to the spatial variability in herbaceous species’ phenology by at the same time considering their functional traits to predict their general and species-specific responses to future climate change. In this project, we analysed phenology records of 148 herbaceous species, which were observed for a single year by the PhenObs network in 15 botanical gardens. For each species, we characterised the spatial variability in six different phenological stages across gardens. We used boosted regression trees to link these variabilities in phenology to the variability in environmental parameters (temperature, latitude, and local habitat conditions) as well as species traits (seed mass, vegetative height, specific leaf area, and temporal niche) hypothesised to be related to phenology variability. We found that spatial variability in the phenology of herbaceous species was mainly driven by the variability in temperature but also photoperiod was an important driving factor for some phenological stages. In addition, we found that early-flowering and less competitive species indicated by small specific leaf area and vegetative height were more variable in their phenology. Our findings contribute to the field of phenology by showing that besides temperature, photoperiod and functional traits are important to be included when spatial variability of herbaceous species is investigated.

    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/10.2...arrow_drop_down
    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/10.21203/rs.3....
    Article . 2023 . Peer-reviewed
    License: CC BY
    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/
    International Journal of Biometeorology
    Article . 2024 . Peer-reviewed
    License: CC BY
    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/
    https://dx.doi.org/10.17169/re...
    Other literature type . 2024
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    Data sources: Datacite
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    PubMed Central
    Other literature type . 2024
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    DIGITAL.CSIC
    Article . 2024 . Peer-reviewed
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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/
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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/ https://doi.org/10.2...arrow_drop_down
      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/10.21203/rs.3....
      Article . 2023 . Peer-reviewed
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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/
      International Journal of Biometeorology
      Article . 2024 . Peer-reviewed
      License: CC BY
      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/
      https://dx.doi.org/10.17169/re...
      Other literature type . 2024
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      DIGITAL.CSIC
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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: Robert Rauschkolb; Solveig Franziska Bucher; Isabell Hensen; Antje Ahrends; +30 Authors

    Abstract Whereas temporal variability of plant phenology in response to climate change has already been well studied, the spatial variability of phenology is not well understood. Given that phenological shifts may affect the magnitude of biotic interactions, there is a need to investigate how the variability in environmental factors relates to the spatial variability in herbaceous species’ phenology by at the same time considering their functional traits to predict their general and species-specific responses to future climate change. In this project, we analysed phenology records of 148 herbaceous species, which were observed for a single year by the PhenObs network in 15 botanical gardens. For each species, we characterised the spatial variability in six different phenological stages across gardens. We used boosted regression trees to link these variabilities in phenology to the variability in environmental parameters (temperature, latitude, and local habitat conditions) as well as species traits (seed mass, vegetative height, specific leaf area, and temporal niche) hypothesised to be related to phenology variability. We found that spatial variability in the phenology of herbaceous species was mainly driven by the variability in temperature but also photoperiod was an important driving factor for some phenological stages. In addition, we found that early-flowering and less competitive species indicated by small specific leaf area and vegetative height were more variable in their phenology. Our findings contribute to the field of phenology by showing that besides temperature, photoperiod and functional traits are important to be included when spatial variability of herbaceous species is investigated.

    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/10.2...arrow_drop_down
    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/10.21203/rs.3....
    Article . 2023 . Peer-reviewed
    License: CC BY
    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/
    International Journal of Biometeorology
    Article . 2024 . Peer-reviewed
    License: CC BY
    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/
    https://dx.doi.org/10.17169/re...
    Other literature type . 2024
    License: CC BY
    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/
    PubMed Central
    Other literature type . 2024
    License: CC BY
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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/
    DIGITAL.CSIC
    Article . 2024 . Peer-reviewed
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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/ https://doi.org/10.2...arrow_drop_down
      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/10.21203/rs.3....
      Article . 2023 . Peer-reviewed
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      International Journal of Biometeorology
      Article . 2024 . Peer-reviewed
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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/
      https://dx.doi.org/10.17169/re...
      Other literature type . 2024
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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/
      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/
      DIGITAL.CSIC
      Article . 2024 . Peer-reviewed
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    Authors: Ulisse Gomarasca; Mirco Migliavacca; Jens Kattge; Jacob A. Nelson; +40 Authors

    AbstractFundamental axes of variation in plant traits result from trade-offs between costs and benefits of resource-use strategies at the leaf scale. However, it is unclear whether similar trade-offs propagate to the ecosystem level. Here, we test whether trait correlation patterns predicted by three well-known leaf- and plant-level coordination theories – the leaf economics spectrum, the global spectrum of plant form and function, and the least-cost hypothesis – are also observed between community mean traits and ecosystem processes. We combined ecosystem functional properties from FLUXNET sites, vegetation properties, and community mean plant traits into three corresponding principal component analyses. We find that the leaf economics spectrum (90 sites), the global spectrum of plant form and function (89 sites), and the least-cost hypothesis (82 sites) all propagate at the ecosystem level. However, we also find evidence of additional scale-emergent properties. Evaluating the coordination of ecosystem functional properties may aid the development of more realistic global dynamic vegetation models with critical empirical data, reducing the uncertainty of climate change projections.

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    Nature Communications
    Article . 2023 . Peer-reviewed
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    https://doi.org/10.21203/rs.3....
    Article . 2023 . Peer-reviewed
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    CNR ExploRA
    Article . 2023
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    Article . 2023
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    Nature Communications
    Article . 2023 . Peer-reviewed
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    Authors: Ulisse Gomarasca; Mirco Migliavacca; Jens Kattge; Jacob A. Nelson; +40 Authors

    AbstractFundamental axes of variation in plant traits result from trade-offs between costs and benefits of resource-use strategies at the leaf scale. However, it is unclear whether similar trade-offs propagate to the ecosystem level. Here, we test whether trait correlation patterns predicted by three well-known leaf- and plant-level coordination theories – the leaf economics spectrum, the global spectrum of plant form and function, and the least-cost hypothesis – are also observed between community mean traits and ecosystem processes. We combined ecosystem functional properties from FLUXNET sites, vegetation properties, and community mean plant traits into three corresponding principal component analyses. We find that the leaf economics spectrum (90 sites), the global spectrum of plant form and function (89 sites), and the least-cost hypothesis (82 sites) all propagate at the ecosystem level. However, we also find evidence of additional scale-emergent properties. Evaluating the coordination of ecosystem functional properties may aid the development of more realistic global dynamic vegetation models with critical empirical data, reducing the uncertainty of climate change projections.

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    Nature Communications
    Article . 2023 . Peer-reviewed
    License: CC BY
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    https://doi.org/10.21203/rs.3....
    Article . 2023 . Peer-reviewed
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    CNR ExploRA
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    Nature Communications
    Article . 2023
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    Article . 2023
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    Article . 2023
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    HAL INRAE
    Article . 2023
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    Nature Communications
    Article . 2023 . Peer-reviewed
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    Article . 2023
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    Authors: Simone Cesarz; Nico Eisenhauer; Solveig Franziska Bucher; Marcel Ciobanu; +1 Authors

    Artificial light at night (ALAN) is increasing worldwide, but its effects on the soil system have not yet been investigated. We tested the influence of experimental manipulation of ALAN on two taxa of soil communities (microorganisms and soil nematodes) and three aspects of soil functioning (soil basal respiration, soil microbial biomass and carbon use efficiency) over four and a half months in a highly controlled Ecotron facility. We show that during peak plant biomass, increasing ALAN reduced plant biomass and was also associated with decreased soil water content. This further reduced soil respiration under high ALAN at peak plant biomass, but microbial communities maintained stable biomass across different levels of ALAN and times, demonstrating higher microbial carbon use efficiency under high ALAN. While ALAN did not affect microbial community structure, the abundance of plant-feeding nematodes increased and there was homogenization of nematode communities under higher levels of ALAN, indicating that soil communities may be more vulnerable to additional disturbances at high ALAN. In summary, the effects of ALAN reach into the soil system by altering soil communities and ecosystem functions, and these effects are mediated by changes in plant productivity and soil water content at peak plant biomass. This article is part of the theme issue ‘Light pollution in complex ecological systems’.

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    Philosophical Transactions of the Royal Society B Biological Sciences
    Article . 2023 . Peer-reviewed
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    Authors: Simone Cesarz; Nico Eisenhauer; Solveig Franziska Bucher; Marcel Ciobanu; +1 Authors

    Artificial light at night (ALAN) is increasing worldwide, but its effects on the soil system have not yet been investigated. We tested the influence of experimental manipulation of ALAN on two taxa of soil communities (microorganisms and soil nematodes) and three aspects of soil functioning (soil basal respiration, soil microbial biomass and carbon use efficiency) over four and a half months in a highly controlled Ecotron facility. We show that during peak plant biomass, increasing ALAN reduced plant biomass and was also associated with decreased soil water content. This further reduced soil respiration under high ALAN at peak plant biomass, but microbial communities maintained stable biomass across different levels of ALAN and times, demonstrating higher microbial carbon use efficiency under high ALAN. While ALAN did not affect microbial community structure, the abundance of plant-feeding nematodes increased and there was homogenization of nematode communities under higher levels of ALAN, indicating that soil communities may be more vulnerable to additional disturbances at high ALAN. In summary, the effects of ALAN reach into the soil system by altering soil communities and ecosystem functions, and these effects are mediated by changes in plant productivity and soil water content at peak plant biomass. This article is part of the theme issue ‘Light pollution in complex ecological systems’.

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    Philosophical Transactions of the Royal Society B Biological Sciences
    Article . 2023 . Peer-reviewed
    License: CC BY
    Data sources: Crossref
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    Authors: Bucher, Solveig Franziska; Uhde, Lia; Weigelt, Alexandra; Cesarz, Simone; +5 Authors

    The EcoUnits were filled with 1.23 m3 of unsterilised, well-mixed soil from the vicinity of the EcoTron, as we also monitored soil communities in the same experimental setup (see Cesarz et al.). Plant communities comprising 16 plant species were sown into soil on 19 February 2020 (see Table S1). Because the soil was not sterilised, some of the local seed bank was also transferred into our experiment. Plant communities were harvested by clipping aboveground plant biomass (2 cm above topsoil) on June 11, July 3, and August 28 (establishment period), as well as on October 27 and December 8 (measurement period). This harvest regime mimics typical intensive grassland management in central Europe, with short growth phases in between harvest events. For this study, we analysed the last two harvests in detail to address temporal variations and accumulated effects of the ALAN treatment (see Table S1; hereafter referred to harvest 1 and 2, respectively). The harvests differed in length: harvest 1 encompassed a time for regrowth of 9 weeks, whereas harvest 2 only encompassed 6 weeks, as this was embedded in a bigger experimental setup. The biomass of one-eighth (0.19 m2) of each EcoUnit (subplot) was separated into species (both sown and not sown as well as ‘unknown’) and then dried to constant weight at 60°C for three days. Plant identification was sometimes not possible when the plants were not fully mature. These species were all clustered as ‘unknown species’, whereas for others only the genus could be determined. Dead biomass was also recorded. Plant functional trait data was collected for one species each per functional group of grasses (B. hordeaceus), non-legume forbs (P. lanceolata) and legumes (T. repens) just before the harvests in October and December. The species were selected based on their frequent occurrence in the EcoUnits. However, not all plant traits were measured on all species and in all EcoUnits. P. lanceolata was originally not sown into the communities but had become one of the dominant species in the EcoUnits by October and was thus selected for our experiment. It was not very abundant by the end of the experiment as it did not regenerate well after the harvest in October. All traits were collected and measured just before the harvest unless stated otherwise. Stretched plant height of three representative individuals per species and EcoUnit was measured using a ruler. Then, ten healthy leaves from at least three manually randomly selected individuals per species and EcoUnit were harvested and transported to the laboratory, where SLA, LDMC, toughness, hairiness and wettability were measured. All ten leaves were scanned on an Epson Expression 11000 XL scanner and the resulting images were analysed using ImageJ to determine the leaf area. In the case of T. repens, only the lamina was scanned. Leaves were weighed and subsequently dried at 70°C for at least 48h, and dry weight was recorded to calculate SLA (leaf area of fresh leaf/ dry weight) and LDMC (dry weight/ fresh weight). All weights were measured using a precision scale (QUINTIX315_1S, Sartorius Lab Instruments GmbH & Co. KG, Goettingen, Germany). A few days afterwards, the chlorophyll fluorescence measurements and the SPAD values were determined on living plants in the EcoUnits, just before the harvests. The hairiness, or rather the density of trichomes, of the leaves was analysed by counting the hairs from an image taken at 400-fold magnification using a light microscope and focussing on the middle part of the leaf (Ocular 10x/22, Di-Li-2009, Distelkamp-Electronic, Kaiserslautern, Germany) in ImageJ. For that, four of the leaves used in SLA measurements were chosen at random. Hairs were counted on the upper and lower leaf side and then added to make a total for both leaf sites. T. repens did not show any hair on its lamina. The samples of this species were excluded from the subsequent analysis. The leaf thickness was measured with a digital caliper (WEZU Messwerkzeuge Remscheid GmbH, Remscheid, Germany) at the same spot as leaf toughness. For leaf toughness, the puncture resistance was measured using a surgical blade at a speed of 129 mm min-1 on an electric test stand (Sauter GmbH, Wutöschingen, Germany) and the force of the cut was measured with a power meter (FH 50, Sauter GmbH). The leaf toughness was than calculated as the quotient between the puncture resistance and the thickness. The leaf wettability was investigated via measuring the contact angle (CA) of a water droplet and the leaf, where high CA means low wettability. For that, a droplet of 5 µl distilled water was placed on a flat leaf surface for 90 seconds and then photographed (Nikon D5300 with a Sigma DC Objective, Chiyoda, Tokyo, Japan). The CA was then measured using ImageJ. Chlorophyll fluorescence was measured using a PocketPEA device (Hansatech, King’s Lynn, Norfolk, UK). We measured the parameters PIabs as well as plant stress via Fv/Fm after 30 min of dark adaption to ensure a full reduction of the photosystems on three replicate individuals for each EcoUnit and species. These measurements were not performed on P. lanceolata, as not many individuals were abundant after harvesting the leaves for the previous analysis. The SPAD value was measured using a SPAD 502 (Minolta Camera Co., Osaka, Japan) on the same individual. For each individual, three replicate measurements were performed as the values varied within individuals. # Artificial light at night (ALAN) decreases plant diversity and performance in experimental grassland communities – Data on species biomass and traits [https://doi.org/10.5061/dryad.hhmgqnknt](https://doi.org/10.5061/dryad.hhmgqnknt) In ALAN\_specis\_biomass.csv, Biomass per species in the proportion sorted is given. In ALAN\_biomass.csv, the biomass of the entire Ecotron is given. In ALAN\_traits.csv, traits of the species are given. ## Description of the data and file structure ALAN\_specis\_biomass.csv: The species are abbreviated by 3 letters genus and species. unit describes the name of the EcoUnit (numbered consecutively), light refers to the light regime (given in lux), mass indicates the biomass (in g dry matter) and harvest denotes whether it was the first or 2nd harvest studied (categorical information). ALAN\_biomass.csv: biomass refers to biomass (g dry matter), unit describes the name of the EcoUnit (numbered consecutively), and harvest denotes whether it was the first or 2nd harvest studied. Treatment refers to the light regime (in lux). ALAN\_traits.csv: Species and EcoUnit are given as above. Treatment refers to the light regime (in lux).. Hair density is hairiness (hairs mm-2), besides that toughness (N mm-1), contact angle (CA\_Mean, °), fresh weight (g), dry weight (g), leaf area (cm2), specific leaf area (SLA; cm2 g-1), leaf dry matter content (mg g-1), SPAD, plant height (cm) and the chlorophyll parameters FvFm and PIabs are given as described in Methods. Artificial light at night (ALAN) affects many areas of the world and is increasing globally. To date, there has been limited and inconsistent evidence regarding the consequences of ALAN on plant communities as well as the fitness of their constituent species. ALAN could be beneficial for plants as they need light as an energy source, but they also need darkness for regeneration and growth. We created model communities composed of 16 plant species sown, exposed to a gradient of ALAN ranging from ‘moonlight only’ to conditions like situations typically found directly underneath a streetlamp. We measured plant community composition and its production (biomass), as well as functional traits of three plant species from different functional groups (grasses, herbs, legumes) in two separate harvests. We found that biomass was reduced by 33% in the highest ALAN treatment compared to the control, Shannon diversity decreased by 43% and Evenness by 34% in the first harvest. Some species failed to establish in the second harvest. Specific leaf area, leaf dry matter content and leaf hairiness responded to ALAN. These responses suggest that plant communities will be sensitive to increasing ALAN, and they flag a need for plant conservation activities that consider impending ALAN scenarios.

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    ZENODO
    Dataset . 2023
    License: CC 0
    Data sources: ZENODO
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    ZENODO
    Dataset . 2023
    License: CC 0
    Data sources: ZENODO
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    Dataset . 2023
    License: CC 0
    Data sources: Datacite
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      ZENODO
      Dataset . 2023
      License: CC 0
      Data sources: ZENODO
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      ZENODO
      Dataset . 2023
      License: CC 0
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      Dataset . 2023
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    Authors: Bucher, Solveig Franziska; Uhde, Lia; Weigelt, Alexandra; Cesarz, Simone; +5 Authors

    The EcoUnits were filled with 1.23 m3 of unsterilised, well-mixed soil from the vicinity of the EcoTron, as we also monitored soil communities in the same experimental setup (see Cesarz et al.). Plant communities comprising 16 plant species were sown into soil on 19 February 2020 (see Table S1). Because the soil was not sterilised, some of the local seed bank was also transferred into our experiment. Plant communities were harvested by clipping aboveground plant biomass (2 cm above topsoil) on June 11, July 3, and August 28 (establishment period), as well as on October 27 and December 8 (measurement period). This harvest regime mimics typical intensive grassland management in central Europe, with short growth phases in between harvest events. For this study, we analysed the last two harvests in detail to address temporal variations and accumulated effects of the ALAN treatment (see Table S1; hereafter referred to harvest 1 and 2, respectively). The harvests differed in length: harvest 1 encompassed a time for regrowth of 9 weeks, whereas harvest 2 only encompassed 6 weeks, as this was embedded in a bigger experimental setup. The biomass of one-eighth (0.19 m2) of each EcoUnit (subplot) was separated into species (both sown and not sown as well as ‘unknown’) and then dried to constant weight at 60°C for three days. Plant identification was sometimes not possible when the plants were not fully mature. These species were all clustered as ‘unknown species’, whereas for others only the genus could be determined. Dead biomass was also recorded. Plant functional trait data was collected for one species each per functional group of grasses (B. hordeaceus), non-legume forbs (P. lanceolata) and legumes (T. repens) just before the harvests in October and December. The species were selected based on their frequent occurrence in the EcoUnits. However, not all plant traits were measured on all species and in all EcoUnits. P. lanceolata was originally not sown into the communities but had become one of the dominant species in the EcoUnits by October and was thus selected for our experiment. It was not very abundant by the end of the experiment as it did not regenerate well after the harvest in October. All traits were collected and measured just before the harvest unless stated otherwise. Stretched plant height of three representative individuals per species and EcoUnit was measured using a ruler. Then, ten healthy leaves from at least three manually randomly selected individuals per species and EcoUnit were harvested and transported to the laboratory, where SLA, LDMC, toughness, hairiness and wettability were measured. All ten leaves were scanned on an Epson Expression 11000 XL scanner and the resulting images were analysed using ImageJ to determine the leaf area. In the case of T. repens, only the lamina was scanned. Leaves were weighed and subsequently dried at 70°C for at least 48h, and dry weight was recorded to calculate SLA (leaf area of fresh leaf/ dry weight) and LDMC (dry weight/ fresh weight). All weights were measured using a precision scale (QUINTIX315_1S, Sartorius Lab Instruments GmbH & Co. KG, Goettingen, Germany). A few days afterwards, the chlorophyll fluorescence measurements and the SPAD values were determined on living plants in the EcoUnits, just before the harvests. The hairiness, or rather the density of trichomes, of the leaves was analysed by counting the hairs from an image taken at 400-fold magnification using a light microscope and focussing on the middle part of the leaf (Ocular 10x/22, Di-Li-2009, Distelkamp-Electronic, Kaiserslautern, Germany) in ImageJ. For that, four of the leaves used in SLA measurements were chosen at random. Hairs were counted on the upper and lower leaf side and then added to make a total for both leaf sites. T. repens did not show any hair on its lamina. The samples of this species were excluded from the subsequent analysis. The leaf thickness was measured with a digital caliper (WEZU Messwerkzeuge Remscheid GmbH, Remscheid, Germany) at the same spot as leaf toughness. For leaf toughness, the puncture resistance was measured using a surgical blade at a speed of 129 mm min-1 on an electric test stand (Sauter GmbH, Wutöschingen, Germany) and the force of the cut was measured with a power meter (FH 50, Sauter GmbH). The leaf toughness was than calculated as the quotient between the puncture resistance and the thickness. The leaf wettability was investigated via measuring the contact angle (CA) of a water droplet and the leaf, where high CA means low wettability. For that, a droplet of 5 µl distilled water was placed on a flat leaf surface for 90 seconds and then photographed (Nikon D5300 with a Sigma DC Objective, Chiyoda, Tokyo, Japan). The CA was then measured using ImageJ. Chlorophyll fluorescence was measured using a PocketPEA device (Hansatech, King’s Lynn, Norfolk, UK). We measured the parameters PIabs as well as plant stress via Fv/Fm after 30 min of dark adaption to ensure a full reduction of the photosystems on three replicate individuals for each EcoUnit and species. These measurements were not performed on P. lanceolata, as not many individuals were abundant after harvesting the leaves for the previous analysis. The SPAD value was measured using a SPAD 502 (Minolta Camera Co., Osaka, Japan) on the same individual. For each individual, three replicate measurements were performed as the values varied within individuals. # Artificial light at night (ALAN) decreases plant diversity and performance in experimental grassland communities – Data on species biomass and traits [https://doi.org/10.5061/dryad.hhmgqnknt](https://doi.org/10.5061/dryad.hhmgqnknt) In ALAN\_specis\_biomass.csv, Biomass per species in the proportion sorted is given. In ALAN\_biomass.csv, the biomass of the entire Ecotron is given. In ALAN\_traits.csv, traits of the species are given. ## Description of the data and file structure ALAN\_specis\_biomass.csv: The species are abbreviated by 3 letters genus and species. unit describes the name of the EcoUnit (numbered consecutively), light refers to the light regime (given in lux), mass indicates the biomass (in g dry matter) and harvest denotes whether it was the first or 2nd harvest studied (categorical information). ALAN\_biomass.csv: biomass refers to biomass (g dry matter), unit describes the name of the EcoUnit (numbered consecutively), and harvest denotes whether it was the first or 2nd harvest studied. Treatment refers to the light regime (in lux). ALAN\_traits.csv: Species and EcoUnit are given as above. Treatment refers to the light regime (in lux).. Hair density is hairiness (hairs mm-2), besides that toughness (N mm-1), contact angle (CA\_Mean, °), fresh weight (g), dry weight (g), leaf area (cm2), specific leaf area (SLA; cm2 g-1), leaf dry matter content (mg g-1), SPAD, plant height (cm) and the chlorophyll parameters FvFm and PIabs are given as described in Methods. Artificial light at night (ALAN) affects many areas of the world and is increasing globally. To date, there has been limited and inconsistent evidence regarding the consequences of ALAN on plant communities as well as the fitness of their constituent species. ALAN could be beneficial for plants as they need light as an energy source, but they also need darkness for regeneration and growth. We created model communities composed of 16 plant species sown, exposed to a gradient of ALAN ranging from ‘moonlight only’ to conditions like situations typically found directly underneath a streetlamp. We measured plant community composition and its production (biomass), as well as functional traits of three plant species from different functional groups (grasses, herbs, legumes) in two separate harvests. We found that biomass was reduced by 33% in the highest ALAN treatment compared to the control, Shannon diversity decreased by 43% and Evenness by 34% in the first harvest. Some species failed to establish in the second harvest. Specific leaf area, leaf dry matter content and leaf hairiness responded to ALAN. These responses suggest that plant communities will be sensitive to increasing ALAN, and they flag a need for plant conservation activities that consider impending ALAN scenarios.

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    ZENODO
    Dataset . 2023
    License: CC 0
    Data sources: ZENODO
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    ZENODO
    Dataset . 2023
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    Data sources: ZENODO
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    Dataset . 2023
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    Data sources: Datacite
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      ZENODO
      Dataset . 2023
      License: CC 0
      Data sources: ZENODO
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      ZENODO
      Dataset . 2023
      License: CC 0
      Data sources: ZENODO
      DRYAD
      Dataset . 2023
      License: CC 0
      Data sources: Datacite
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    Authors: Maria Sporbert; Desiree Jakubka; Solveig Franziska Bucher; Isabell Hensen; +19 Authors

    Summary Phenology has emerged as key indicator of the biological impacts of climate change, yet the role of functional traits constraining variation in herbaceous species’ phenology has received little attention. Botanical gardens are ideal places in which to investigate large numbers of species growing under common climate conditions. We ask whether interspecific variation in plant phenology is influenced by differences in functional traits. We recorded onset, end, duration and intensity of initial growth, leafing out, leaf senescence, flowering and fruiting for 212 species across five botanical gardens in Germany. We measured functional traits, including plant height, absolute and specific leaf area, leaf dry matter content, leaf carbon and nitrogen content and seed mass and accounted for species’ relatedness. Closely related species showed greater similarities in timing of phenological events than expected by chance, but species' traits had a high degree of explanatory power, pointing to paramount importance of species’ life‐history strategies. Taller plants showed later timing of initial growth, and flowered, fruited and underwent leaf senescence later. Large‐leaved species had shorter flowering and fruiting durations. Taller, large‐leaved species differ in their phenology and are more competitive than smaller, small‐leaved species. We assume climate warming will change plant communities’ competitive hierarchies with consequences for biodiversity.

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    New Phytologist
    Article . 2022 . Peer-reviewed
    License: CC BY
    Data sources: Crossref
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    https://dx.doi.org/10.17169/re...
    Other literature type . 2022
    License: CC BY
    Data sources: Datacite
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    MPG.PuRe
    Article . 2022
    Data sources: MPG.PuRe
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    New Phytologist
    Article . 2022
    New Phytologist
    Article . 2022
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    Authors: Maria Sporbert; Desiree Jakubka; Solveig Franziska Bucher; Isabell Hensen; +19 Authors

    Summary Phenology has emerged as key indicator of the biological impacts of climate change, yet the role of functional traits constraining variation in herbaceous species’ phenology has received little attention. Botanical gardens are ideal places in which to investigate large numbers of species growing under common climate conditions. We ask whether interspecific variation in plant phenology is influenced by differences in functional traits. We recorded onset, end, duration and intensity of initial growth, leafing out, leaf senescence, flowering and fruiting for 212 species across five botanical gardens in Germany. We measured functional traits, including plant height, absolute and specific leaf area, leaf dry matter content, leaf carbon and nitrogen content and seed mass and accounted for species’ relatedness. Closely related species showed greater similarities in timing of phenological events than expected by chance, but species' traits had a high degree of explanatory power, pointing to paramount importance of species’ life‐history strategies. Taller plants showed later timing of initial growth, and flowered, fruited and underwent leaf senescence later. Large‐leaved species had shorter flowering and fruiting durations. Taller, large‐leaved species differ in their phenology and are more competitive than smaller, small‐leaved species. We assume climate warming will change plant communities’ competitive hierarchies with consequences for biodiversity.

    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/ New Phytologistarrow_drop_down
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    New Phytologist
    Article . 2022 . Peer-reviewed
    License: CC BY
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    https://dx.doi.org/10.17169/re...
    Other literature type . 2022
    License: CC BY
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    MPG.PuRe
    Article . 2022
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    New Phytologist
    Article . 2022
    New Phytologist
    Article . 2022
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    Authors: Solveig Franziska Bucher; Lia Uhde; Alexandra Weigelt; Simone Cesarz; +6 Authors

    Artificial light at night (ALAN) affects many areas of the world and is increasing globally. To date, there has been limited and inconsistent evidence regarding the consequences of ALAN for plant communities, as well as for the fitness of their constituent species. ALAN could be beneficial for plants as they need light as energy source, but they also need darkness for regeneration and growth. We created model communities composed of 16 plant species sown, exposed to a gradient of ALAN ranging from ‘moonlight only’ to conditions like situations typically found directly underneath a streetlamp. We measured plant community composition and its production (biomass), as well as functional traits of three plant species from different functional groups (grasses, herbs, legumes) in two separate harvests. We found that biomass was reduced by 33% in the highest ALAN treatment compared to the control, Shannon diversity decreased by 43% and evenness by 34% in the first harvest. Some species failed to establish in the second harvest. Specific leaf area, leaf dry matter content and leaf hairiness responded to ALAN. These responses suggest that plant communities will be sensitive to increasing ALAN, and they flag a need for plant conservation activities that consider impending ALAN scenarios.This article is part of the theme issue ‘Light pollution in complex ecological systems’.

    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/ Philosophical Transa...arrow_drop_down
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    Philosophical Transactions of the Royal Society B Biological Sciences
    Article . 2023 . Peer-reviewed
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    Authors: Solveig Franziska Bucher; Lia Uhde; Alexandra Weigelt; Simone Cesarz; +6 Authors

    Artificial light at night (ALAN) affects many areas of the world and is increasing globally. To date, there has been limited and inconsistent evidence regarding the consequences of ALAN for plant communities, as well as for the fitness of their constituent species. ALAN could be beneficial for plants as they need light as energy source, but they also need darkness for regeneration and growth. We created model communities composed of 16 plant species sown, exposed to a gradient of ALAN ranging from ‘moonlight only’ to conditions like situations typically found directly underneath a streetlamp. We measured plant community composition and its production (biomass), as well as functional traits of three plant species from different functional groups (grasses, herbs, legumes) in two separate harvests. We found that biomass was reduced by 33% in the highest ALAN treatment compared to the control, Shannon diversity decreased by 43% and evenness by 34% in the first harvest. Some species failed to establish in the second harvest. Specific leaf area, leaf dry matter content and leaf hairiness responded to ALAN. These responses suggest that plant communities will be sensitive to increasing ALAN, and they flag a need for plant conservation activities that consider impending ALAN scenarios.This article is part of the theme issue ‘Light pollution in complex ecological systems’.

    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/ Philosophical Transa...arrow_drop_down
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    Philosophical Transactions of the Royal Society B Biological Sciences
    Article . 2023 . Peer-reviewed
    License: CC BY
    Data sources: Crossref
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