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Search: WFRF:(Lang S.) > Swedish University of Agricultural Sciences

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  • Poyatos, R., et al. (author)
  • Global transpiration data from sap flow measurements: the SAPFLUXNET database
  • 2021
  • In: Earth System Science Data. - : Copernicus GmbH. - 1866-3508 .- 1866-3516. ; 13:6, s. 2607-2649
  • Journal article (peer-reviewed)abstract
    • Plant transpiration links physiological responses of vegetation to water supply and demand with hydrological, energy, and carbon budgets at the land-atmosphere interface. However, despite being the main land evaporative flux at the global scale, transpiration and its response to environmental drivers are currently not well constrained by observations. Here we introduce the first global compilation of whole-plant transpiration data from sap flow measurements (SAPFLUXNET, https://sapfluxnet.creaf.cat/, last access: 8 June 2021). We harmonized and quality-controlled individual datasets supplied by contributors worldwide in a semi-automatic data workflow implemented in the R programming language. Datasets include sub-daily time series of sap flow and hydrometeorological drivers for one or more growing seasons, as well as metadata on the stand characteristics, plant attributes, and technical details of the measurements. SAPFLUXNET contains 202 globally distributed datasets with sap flow time series for 2714 plants, mostly trees, of 174 species. SAPFLUXNET has a broad bioclimatic coverage, with woodland/shrubland and temperate forest biomes especially well represented (80 % of the datasets). The measurements cover a wide variety of stand structural characteristics and plant sizes. The datasets encompass the period between 1995 and 2018, with 50 % of the datasets being at least 3 years long. Accompanying radiation and vapour pressure deficit data are available for most of the datasets, while on-site soil water content is available for 56 % of the datasets. Many datasets contain data for species that make up 90 % or more of the total stand basal area, allowing the estimation of stand transpiration in diverse ecological settings. SAPFLUXNET adds to existing plant trait datasets, ecosystem flux networks, and remote sensing products to help increase our understanding of plant water use, plant responses to drought, and ecohydrological processes. SAPFLUXNET version 0.1.5 is freely available from the Zenodo repository (https://doi.org/10.5281/zenodo.3971689; Poyatos et al., 2020a). The "sapfluxnetr" R package - designed to access, visualize, and process SAPFLUXNET data - is available from CRAN.
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3.
  • Keogan, Katharine, et al. (author)
  • Global phenological insensitivity to shifting ocean temperatures among seabirds
  • 2018
  • In: Nature Climate Change. - : Springer Science and Business Media LLC. - 1758-678X .- 1758-6798. ; 8:4, s. 313-318
  • Journal article (peer-reviewed)abstract
    • Reproductive timing in many taxa plays a key role in determining breeding productivity(1), and is often sensitive to climatic conditions(2). Current climate change may alter the timing of breeding at different rates across trophic levels, potentially resulting in temporal mismatch between the resource requirements of predators and their prey(3). This is of particular concern for higher-trophic-level organisms, whose longer generation times confer a lower rate of evolutionary rescue than primary producers or consumers(4). However, the disconnection between studies of ecological change in marine systems makes it difficult to detect general changes in the timing of reproduction(5). Here, we use a comprehensive meta-analysis of 209 phenological time series from 145 breeding populations to show that, on average, seabird populations worldwide have not adjusted their breeding seasons over time (-0.020 days yr(-1)) or in response to sea surface temperature (SST) (-0.272 days degrees C-1) between 1952 and 2015. However, marked between-year variation in timing observed in resident species and some Pelecaniformes and Suliformes (cormorants, gannets and boobies) may imply that timing, in some cases, is affected by unmeasured environmental conditions. This limited temperature-mediated plasticity of reproductive timing in seabirds potentially makes these top predators highly vulnerable to future mismatch with lower-trophic-level resources(2).
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4.
  • Lang, Andreas, et al. (author)
  • Monitoring environmental effects on farmland Lepidoptera : Does necessary sampling effort vary between different bio-geographic regions in Europe?
  • 2019
  • In: Ecological Indicators. - : Elsevier BV. - 1470-160X .- 1872-7034. ; 102, s. 791-800
  • Journal article (peer-reviewed)abstract
    • In agro-ecosystems, environmental monitoring is fundamental to detect and survey changes related to land use change and management practices. Butterflies and moths have often been suggested as suitable indicators for monitoring environmental effects on biodiversity in farmlands. Here, we estimated the required sample size and monitoring effort necessary to run a Lepidoptera survey in European farmland, assessing in particular if monitoring investment would differ between representative bio-geographical regions. We operated linear 1-km long transect routes in farmland of Romania, Spain and Sweden from 2013 to 2015, and recorded butterflies and burnet moths (Papilionoidea, Zygaenidae). The transects were walked back and forth four times a season, and replicated yearly. The lepidopteran diversity was high in farmlands of Romania and Spain, but comparatively low in Sweden. The coefficient of variation (CV) of recorded species number differed between countries being lowest in Sweden and highest in Spain. In general, the CV dropped above a transect length of 400–800 m, thus indicating an increase in statistical power. Assuming a non-parametric test for matched samples, power calculations were conducted with the raw count data and with log-transformed count data for comparison. When using log-transformed data, the required sample size to detect an effect was less than 10 transects per country or region (in order to detect a 10% loss of species or a decrease of 30% in total abundance). Specific subgroups of species, e.g. protected species or specific indicator groups, showed a higher variance, thus requiring a higher sample size to detect effects ranging from 12 to 16 transects (equivalent to 21–29 working days per country and year). When using original, untransformed count data a considerably larger sample size would be needed. Actual time to be invested in field work differed between countries due to contrasting regional constraints and conditions. Nevertheless, the final monitoring effort in working days was similar between countries as the factors involved balanced out each other, in particular due to the differing year-to-year variations. Our study demonstrated the feasibility of an environmental monitoring programme in arable land using farmland butterflies across Europe. We present a suitable approach and guidelines as well as the necessary effort to be invested in future Europe-wide monitoring programmes of butterflies in agro-ecosystems, based on predictions of statistical power.
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