en: rainfall-runoff-modelling precipitation nonlinear-deconvolution streamflow ecohydrology nonstationarity hydrology time-series

en: An introduction to ERRA v1.06.pdf

en: "An introduction to ERRA" presents a series of vignettes that introduce some of the capabilities of the Ensemble Rainfall-Runoff Analysis (ERRA) script, and that show how to invoke them. This introduction also includes documentation for ERRA function calls, largely reproducing the documentation embedded in the ERRA script itself.

en: {{deprecated version}} ERRA_scripts.zip

en: Zip-compressed folder containing two versions of the ERRA script. ERRA_v1.0.R uses Rcpp to speed up several key calculations, but requires a C++ compiler. ERRA_v1.0_no_Rcpp.R is a bit slower but does not require a C++ compiler or Rcpp. Public use of these scripts is permitted under GNU General Public License 3 (GPL3); for details see https://www.gnu.org/licenses/

en: Demonstration scripts.zip

en: Zip-compressed folder containing demonstration scripts, source data, and output files for the ERRA results shown in "Introduction to ERRA" and in J.W. Kirchner, "Characterizing nonlinear, nonstationary, and heterogeneous hydrologic behavior using Ensemble Rainfall-Runoff Analysis (ERRA): proof of concept", Hydrology and Earth System Sciences, 2024.

en: Zip-compressed folder containing two versions of the ERRA script. ERRA_v1.06.R uses Rcpp to speed up several key calculations, but requires a C++ compiler. ERRA_v1.06_no_Rcpp.R is a bit slower but does not require a C++ compiler or Rcpp. Public use of these scripts is permitted under GNU General Public License 3 (GPL3); for details see https://www.gnu.org/licenses/

en: {{deprecated version}} An introduction to ERRA.pdf

en:
ERRA is a data-driven, nonparametric, model-independent method for quantifying rainfall-runoff relationships across a spectrum of time lags, in systems that may be nonlinear, nonstationary, and spatially heterogeneous.
Researchers using ERRA in published work should cite J.W. Kirchner, "Characterizing nonlinear, nonstationary, and heterogeneous hydrologic behavior using Ensemble Rainfall-Runoff Analysis (ERRA): proof of concept", Hydrology and Earth System Sciences, 2024 (for ERRA itself) and J.W. Kirchner, "Impulse response functions for nonlinear, nonstationary, and heterogeneous systems, estimated by deconvolution and de-mixing of noisy time series", Sensors, 22(9), 3291, https://doi.org/10.3390/s22093291, 2022 (for the underlying mathematics).
This data set includes two versions of the ERRA script written in the open-source programming language R, a detailed user's guide, and sample scripts and source data for all of the results in Kirchner (2024).
These scripts are made publicly available under GNU General Public License 3; for details see https://www.gnu.org/licenses/. The data and documentation are made available under Creative Commons Attribution Share-Alike CC-BY-SA.
ETH Zurich, WSL, and James Kirchner make ABSOLUTELY NO WARRANTIES OF ANY KIND, including NO WARRANTIES, expressed or implied, that this software is free of errors or is suitable for any particular purpose. Users are solely responsible for determining the suitability and reliability of this software for their own purposes.

ecohydrology

display_name: ecohydrology

hydrology

display_name: hydrology

nonlinear-deconvolution

display_name: nonlinear-deconvolution

nonstationarity

display_name: nonstationarity

precipitation

display_name: precipitation

rainfall-runoff-modelling

display_name: rainfall-runoff-modelling

streamflow

display_name: streamflow

en: ERRA -- an R script for Ensemble Rainfall-Runoff Analysis


maintainer: Ana Beatriz Pierri Daunt

en: landscape-services landscape-perception socio-ecological-system literature-review pdfsearch sense-of-place green-infrastructure resilience landscape-planning landscape-ecology ecosystem-services multifunctionality planning decision-making

state: active

type: dataset

en: 3. Use of any early concept.

media_type: text/csv

format: CSV

en: 5. Planning steps.

en: 4. Use of any additional concept.

en: 2. Frequency of additional concepts.

en: 6. Protocol

format: XLS

en: 1. Frequency of early concepts.

en:
Table of content: 1. Frequency of early concepts; 2. Frequency of additional concepts; 3. Use of any early concept; 4. Use of any additional concept, 5. Planning steps; 6. Protocol.

The present dataset is part of the published scientific paper entitled “Landscape ecological concepts in planning: review of recent developments” (Hersperger et al., 2021). The goal of this research was to review recent publications to assess the use of landscape ecological concepts in planning. Specifically, we address the following research questions: Q1. Landscape ecological concepts: What are they? How frequently are they mentioned in current research? Q2. How are landscape ecological concepts integrated in landscape planning?

We analysed all empirical and overview papers that have been published in four key academic journals in the field of landscape ecology and landscape planning in the years 2015–2019 (n = 1918). Four key journals in the field of landscape ecology were selected to conduct the analysis, respectively Landscape Ecology (LE), Landscape Online (LO), Current Landscape Ecology Reports (CLER), and Landscape and Urban Planning (LUP). The title, abstract and keywords of all papers were read in order to identify landscape ecological concepts. Then, all 1918 papers went through a keyword search to identify the use of early and additional concepts. We used the “pdfsearch” package in R programming language and searched for singular and plural forms and different variations of the concepts (see Supplementary material 1, Table A). As a result, we provided four outputs:

  1. Frequency of early concepts. This data provides the total number of times each article used each early concept (Q1). This data was used to produce the Figure 2a at the original publication.

  2. Frequency of additional concepts. This data provides the total number of times each article used each additional concept (Q1). This data was used to produce the Figure 2b at the original publication.

  3. Use of any early concept. This data provides the total number of times each article used any early concept (Q1).
This data was used to produce the Figure 3a at the original publication.

  4. Use of any additional concept. This data provides the total number of times each article used any additional concept (Q1). This data was used to produce the Figure 3b at the original publication.

To address the second question (Q2), the title, abstract and keywords of the papers included in our sample (n=1918 articles) were screened to identify papers that might show how landscape ecological concepts are integrated into planning. We selected 52 empirical papers (see Supplementary material – 4 Integration of landscape ecological concepts into planning), and we provided two outputs:

  5. Planning steps. This data provides the number of times landscape ecological concepts were addressed in each
planning steps in 52 empirical papers analysed in detail (Q2). This data was used to produce the Figure 4 at the
original publication.

  6. Protocol for assessing the integration of landscape ecological concepts into planning. To systematically collect the
data, we used this protocol which addressed the following questions: (a) which type of planning is addressed by the
paper? (b) to which planning level does the paper refer to? (c) which concepts are integrated in any of the planning
steps described above?

decision-making

display_name: decision-making

ecosystem-services

display_name: ecosystem-services

green-infrastructure

display_name: green-infrastructure

landscape-ecology

display_name: landscape-ecology

landscape-perception

display_name: landscape-perception

landscape-planning

display_name: landscape-planning

landscape-services

display_name: landscape-services

literature-review

display_name: literature-review

multifunctionality

display_name: multifunctionality

pdfsearch

display_name: pdfsearch

planning

display_name: planning

resilience

display_name: resilience

sense-of-place

display_name: sense-of-place

socio-ecological-system

display_name: socio-ecological-system

educ

fr: Éducation, culture et sport

de: Bildung, Kultur und Sport

en: Education, culture and sport

it: Istruzione, cultura e sport

envidat

fr: EnviDat: le portail de données environnementales

de: EnviDat: das Umwelt-Datenportal

en: EnviDat: the Environmental Data Portal

it: EnviDat: il portale dei dati ambientali

fr: EnviDat est le portail de données du WSL; il offre un accès uniformisé et réglementé aux données de surveillance et de recherche en matière d’environnement. Ce portail est capable d’héberger et de publier des ensembles de données précieuses et uniques, qui sont partagées aux quatre coins de la planète. Ce faisant, EnviDat favorise la recherche et contribue à l’avancement des sciences environnementales.

en: EnviDat is the WSL data portal providing unified and managed access to environmental monitoring and research data. The portal has the capability to host and publish data sets. Through the sharing of unique and high-value data sets worldwide, EnviDat fosters research and contributes to advancing environmental science.

de: EnviDat ist das Datenportal der WSL für einen einheitlichen und verwalteten Zugang zu Umweltdaten aus Monitoring- und Forschungsprojekten. Auf dem Portal können Datensätze gehostet und veröffentlicht werden. Durch die weltweite Bereitstellung einzigartiger und wertvoller Datensätze leistet EnviDat einen Beitrag zur Forschung im Bereich der Umweltwissenschaften.

it: EnviDat è il portale dati del WSL che fornisce un accesso unificato e gestito ai dati di monitoraggio ambientale e di ricerca. Il portale ha la capacità di ospitare e pubblicare serie di dati preziosi e unici che vengono condivisi in tutto il mondo. Così facendo, EnviDat promuove la ricerca e contribuisce al progresso della scienza ambientale.

political_level: other

wsl

capacity: public

type: organization

approval_status: approved

key: guid

key: uri

value: Envidat Harvester

en: The usage of landscape ecological concepts in the planning literature


maintainer: Henning Löwe

en: microstructure discrete-element-modelling spherical-model-snow 3d-ct-images snow-mechanics unconfined-compression-experiments

en: Data Access

format: SERVICE

en: Data Structure (Python Notebook - view online)

en: Data Structure (Python Notebook)

media_type: text/plain

format: TXT

mimetype: text/plain

en:
For the investigation of microstructural and mechanical properties of snow unconfined compression experiments and 3D computed tomography (CT) imaging were performed on sintered rounded grain snow and spherical model snow. The spherical model snow was generated to create geometrically simplified, well-defined microstructures for calibration of numerical models, such as discrete element models (DEM) in which the microstructure is represented by spherical particles.
In the experiments, microstructural variation was created by varying the sintering time (contact size) and the density of the ice sphere samples (number of contacts). The 3D CT images allow for a complete reconstruction of the entire experimental sample (cylindrical sample dimension: diameter = 33.6 mm; height = 14 mm).

discrete-element-modelling

display_name: discrete-element-modelling

microstructure

display_name: microstructure

snow-mechanics

display_name: snow-mechanics

spherical-model-snow

display_name: spherical-model-snow

unconfined-compression-experiments

display_name: unconfined-compression-experiments

en: Unconfined compression experiments and 3D CT images of spherical model snow and RG snow samples


maintainer: Dirk Nikolaus Karger

en: temperature climate-layers climatology climate precipitation bioclim climate-change free-climate-data

en: CHELSA Technical Documentation

media_type: application/pdf

en: Technical documentation document including the variable names, units, scaling, offset, and background.

format: PDF

en: CHELSA V2.1 (current)

en: CHELSA Version 2.1 based on ERA5 forcings and CMIP6

format: GeoTIFF

en: CHELSA V1.2 (deprecated)

en: CHELSA Version 1.2 based on ERA-Interim forcings and CMIP5

en:
High-resolution information on climatic conditions is essential to many applications in environmental and ecological sciences. Here we present the CHELSA (Climatologies at high resolution for the earth’s land surface areas) data of downscaled temperature and precipitation to a high resolution of 30 arc sec. The temperature algorithm is based on statistical downscaling of atmospheric temperatures. The precipitation algorithm incorporates orographic predictors including wind fields, valley exposition, and boundary layer height, with a subsequent bias correction.

CHELSA data published in EnviDat includes the deprecated version 1.2 (originally published under 10.5061/dryad.kd1d4). Please use the current 2.1 version.

Paper Citation:
 > _Karger DN. et al. Climatologies at high resolution for the earth’s land surface areas, Scientific Data, 4, 170122 (2017) [doi: 10.1038/sdata.2017.122](https://doi.org/10.1038/sdata.2017.122)._

bioclim

display_name: bioclim

climate

display_name: climate

climate-change

display_name: climate-change

climate-layers

display_name: climate-layers

climatology

display_name: climatology

free-climate-data

display_name: free-climate-data

precipitation

display_name: precipitation

temperature

display_name: temperature


snow-drift-station-snow-and-air-data

maintainer: Benjamin Walter

title_for_slug: snow-drift-station-snow-and-air-data

en: raclets snow snow-depth temperature snow-height snow-temperature

en: Relative Humidity

en: The relative humidity (%) was measured with a Campbell CS-215 at a height of 2.2 m above ground. The time is given in UTC+1.

en: Air Temperature

en: The air temperature (°C) was measured with a Campbell CS-215 which was mounted at a height of 2.2 m above ground. The time is given in UTC+1.

en: Snow Depth

en: The snow depth (cm) was measured with a Lufft SHM-31 which was mounted at 1.7 m above ground. The time is given in UTC+1.

en: Snow Surface Temperature

en: The snow surface temperature (°C) was measured with a Campbell SI-111 at 0.7 m above ground. The time is given in UTC+1.

en: Snow and air data was monitored at Gotschnagrat (LON: 46.859 LAT: 9.849) by an infrarot radiometer (Campbell SI-111) for snow temperature (°C), a snow height sensor (Lufft SHM-31) for snow height change (cm) and a temperature and humidity sensor (Campbell CS-215) for air temperature (°C) and relative humidity (%). No filter was applied to the sensors and the smapling frequency was 1 Hz.

raclets

display_name: raclets

snow

display_name: snow

snow-depth

display_name: snow-depth

snow-height

display_name: snow-height

snow-temperature

display_name: snow-temperature

educ

en: Education, culture and sport

envidat

en: EnviDat: the Environmental Data Portal

en: Snow Drift Station - Snow and Air Data


maintainer: EnviDat Support

en: spatial-planning land-use-change land-use-simulations land-use-transformations digital-zoning-plans

en: Legend simulated maps

en:
Table of Content: 1. General context of the data set "LUSzoning”; 2. Background and aims of the study using the data set LUSzoning; 3. The data set LUSzoning.
1. General context of the data set "LUSzoning".
The data set "LUSzoning" stands for Land-use simulations integrating zoning regulations in Spanish functional urban areas. The data set has been generated as part of the CONCUR research project (https://www.wsl.ch/en/projects/concur.html) led by Dr. Anna M. Hersperger and funded by the Swiss National Science Foundation (ERC TBS Consolidator Grant (ID: BSCGIO 157789) for the period 2016-2021. The CONCUR research project is interdisciplinary and aims to develop a scientific basis for adequately integrating spatial policies (in this case, digital zoning plans) into quantitative land-change modelling approaches at the urban regional level.
2.	Background and aims of the study using the data set “LUSzoning”.
As part of the CONCUR project, a specific task was to integrate planning spatial policies in land-change modelling. Planning can be implemented in modelling using either hard or gradual restrictions. Different studies have addressed the inclusion of spatial planning policies in land-use change modelling. However, the integration of zoning constraints is generally established as hard or Boolean-based restrictions (e.g., whether urban development is allowed or not), while not accounting for the spatial heterogeneity or gradual characteristics within planning zones (e.g., whether planning regulations allow low, medium or high urban density), though these could improve real patterns simulations in urban areas. We assume Spanish General Zoning plans were suitable to explore the integration of planning into land-change modelling as soft constrains because they define land-use intensities in the buildable zoning areas. In light of the above considerations, the overall aim of the study was to model urban land-use changes using a multi-scenario approach that integrates digitized zoning plans for the Functional Urban Areas (FUAs) of Madrid, Barcelona, Valencia, and Zaragoza. The following specific objectives were addressed: i) to analyse the role of planning by defining three future scenarios that integrate digitized zoning plans and one scenario that assumes almost no planning intervention; ii) to introduce zoning constraints that reflect different degrees of urban densities; iii) to generate a transferable spatially-explicit modelling framework to integrate planning into land-use change simulations.
Four future land-use demands scenarios were defined for the FUAs. Storylines were created considering probable development scenarios related to zoning plans, current Spanish legislation and sustainability goals defined along two axes: a high market-oriented vs. high planning-intervention axis, and an axis of short-term economic growth vs. long-term sustainable growth. The sustainable development scenario (S1) is characterized by low gross floor area (GFA) growth that is limited to areas that are currently under development according to zoning plans. The business-as-usual scenario (S2) is characterized by medium GFA growth in the range of on-going trends. The strong development scenario (S3) is characterized by high GFA growth rates. Growth is restricted to buildable areas without urbanization project designated in zoning plans. The unrestricted development scenario (S4) prioritizes a high degree of market liberalization characterized by high GFA growth that surpasses population demands. S4 follows a rapid economic growth pattern with almost no planning intervention.
3.	 The data set “LUSzoning”.
The dataset includes 16 .asc raster layers providing the simulated land-uses under four defined scenarios for Barcelona, Madrid, Valencia and Zaragoza Functional Urban Areas (FUAs) for 2030. The simulated raster layers were created using CLUMondo simulation framework and have a spatial resolution of 30m. The .asc layers name include the name of the FUA and scenario number. For example, the output from simulating the urban growth for the city of Zaragoza under Scenario 2 is named “Zaragoza_S2.tif”. Furthermore, a .txt file named “Legend.txt” includes the numeric value of the land-use and the category of land-use that represents to interpret the .asc raster layers. The name of the land-use classes is a reclassification of the Urban Atlas 2012 land-use classes within the four Spanish FUAs analyzed.

digital-zoning-plans

display_name: digital-zoning-plans

land-use-change

display_name: land-use-change

land-use-simulations

display_name: land-use-simulations

land-use-transformations

display_name: land-use-transformations

spatial-planning

display_name: spatial-planning

envidat

en: EnviDat is the WSL data portal providing unified and managed access to environmental monitoring and research data. The portal has the capability to host and publish data sets. Through the sharing of unique and high-value data sets worldwide, EnviDat fosters research and contributes to advancing environmental science.

en: LUSzoning: Land-use simulations integrating zoning regulations in Spanish functional urban areas


en: soil-chemistry topsoil-removal soil-biology nematodes restoration soil-biodiversity fungi soil bacteria biodiversity plants grassland

en: Networks

en:
Treatment	Treatment groups; Y.4-18 = restored grasslands; Initial = intensively managed grasslands; Target = species-rich semi-wet to semi-dry grasslands
Correlation	non-parametric Spearman rank correlations
Vertex.1+2	Comparison between network components; N.pool = total soil nitrogen pool [kg ha-1 12 cm-1]; Corg.pool = soil organic carbon pool [kg ha-1 12 cm-1], pH = soil pH [CaCl2]; BD = bulk density [g cm-3]; FC = field capacity [%]
	PCoA 1 + 2 biotic communities [Veg = vegetation; Nem = nematoda; Fun = fungi; Prok = prokaryota]
Type	Interactions type; A.A = abiotic.abiotic; A.B = abiotic.biotic; B.B = biotic.biotic

en: Nematode data

en:
Sample.data
Plot.ID	consecutive numbers for plots (in total 36 plots)
Treatment	One restoration treatment and two reference treatments. Topsoil+Propagules= Topsoil removal (upper 10-30 cm) combined with introduction of target plant species; Initial=intensively managed grasslands; Target= species-rich semi-wet to semi-dry grasslands
treat.yr	Treatment abbreviation. For restored grasslands: Treatment abbreviation + time since restoration; Initial + Target = NA
yr.trt	year when topsoil was removed; Initial + Target = NA
Age	time since restoration (sampling year 2018 - yr.trt); Initial + Target = NA
Age.class	restored sites of similar age grouped into four age classes. Y.4 = Year 3+4 (recently restored); Y.18 = Year 17+19 (mid-term); Y.24 = Year 23+25 (long-term); Y.30 = Year 27+32 (long-term); Initial + Target = NA
Cluster	clustered spatial arrangment of sites in the field (see Supporting Information Fig. S1)
Site	clustered spatial arrangment (replicates) of plots per site (see Supporting Information Fig. S1)

Taxonomy
ASV.ID	unit number.letter code per amplicon sequence variant (in total 904)
Taxonomic rank	Phylum, Class, Order, Family, Genus, Species

Abundance
columns	Plot.ID (see Sample.data)
rows	ASV.ID (see Taxonomy)

en: Soil properties

en:
Plot.ID	consecutive numbers for plots (in total 36 plots)
Treatment	One restoration treatment and two reference treatments. Topsoil+Propagules= Topsoil removal (upper 10-30 cm) combined with introduction of target plant species; Initial=intensively managed grasslands; Target= species-rich semi-wet to semi-dry grasslands
treat.yr	Treatment abbreviation. For restored grasslands: Treatment abbreviation + time since restoration; Initial + Target = NA
yr.trt	year when topsoil was removed; Initial + Target = NA
Age	time since restoration (sampling year 2018 - yr.trt); Initial + Target = NA
Age.class	restored sites of similar age grouped into four age classes. Y.4 = Year 3+4 (recently restored); Y.18 = Year 17+19 (mid-term); Y.24 = Year 23+25 (long-term); Y.30 = Year 27+32 (long-term); Initial + Target = NA
Cluster	clustered spatial arrangment of sites in the field (see Supporting Information Fig. S1)
Site	clustered spatial arrangment (replicates) of plots per site (see Supporting Information Fig. S1)
N.pool	Soil nitrogen pool (June 2017); corrected for bulk density and 12 cm sampling depth [kg ha-1 12cm-1]
Corg.pool	Soil organic carbon pool (June 2017); corrected for bulk density and 12 cm sampling depth [kg ha-1 12cm-1]
pH	soil pH [CaCl2]
BD	Bulk density [g cm-3]
FC	Field capacity [%]
Veg.1	principle coordinate axis 1 (vegetation)
Veg.1	principle coordinate axis 2 (vegetation)
Nem.1	principle coordinate axis 1 (nematoda)
Nem.2	principle coordinate axis 2 (nematoda)
Fun.1	principle coordinate axis 1 (fungi)
Fun.2	principle coordinate axis 2 (fungi)
Prok.1	principle coordinate axis 1 (prokaryota)
Prok.2	principle coordinate axis 2 (prokaryota)
Veg.H	Shannon diversity (vegetation)
Nem.H	Shannon diversity (nematoda)
Fun.H	Shannon diversity (fungi)
Prok.H	Shannon diversity (prokaryota)

en: Ecosystem coupling_interactions

en:
Treatment	Treatment groups; Y.4-18 = restored grasslands; Initial = intensively managed grasslands; Target = species-rich semi-wet to semi-dry grasslands
Type	Interactions type; A.A = abiotic.abiotic; A.B = abiotic.biotic; B.B = biotic.biotic
Correlation	non-parametric Spearman rank correlations between biotic and abiotic parameters (ecological interactions)

en: Distance to target results

en:
Community	biotic community (vegetation, nematoda, fungi, prokaryota)
Treatment	Treatment groups; Y.4-30= restored grasslands (time since restoration); Initial=intensively managed grasslands (I)
Comparison	within- or between-community Bray-Curtis dissimilarity distance comparison
Label	within-community distances of initial/restored grasslands: treatment abbreviation; between-communities distances of initial/restored-to-target grasslands: treatment abbreviation plus Target (T; species-rich grasslands)
mean	Mean distance to Target (6 plots per treatment group)
sd	Standard deviation of distances to Target (6 plots per treatment group)

en: Vegetation data

en:
Plot.ID	consecutive numbers for plots (in total 36 plots)
Treatment	One restoration treatment and two reference treatments. Topsoil+Propagules= Topsoil removal (upper 10-30 cm) combined with introduction of target plant species; Initial=intensively managed grasslands; Target= species-rich semi-wet to semi-dry grasslands
treat.yr	Treatment abbreviation. For restored grasslands: Treatment abbreviation + time since restoration; Initial + Target = NA
yr.trt	year when topsoil was removed; Initial + Target = NA
Age	time since restoration (sampling year 2018 - yr.trt); Initial + Target = NA
Age.class	restored sites of similar age grouped into four age classes. Y.4 = Year 3+4 (recently restored); Y.18 = Year 17+19 (mid-term); Y.24 = Year 23+25 (long-term); Y.30 = Year 27+32 (long-term); Initial + Target = NA
Cluster	clustered spatial arrangment of sites in the field (see Supporting Information Fig. S1)
Site	clustered spatial arrangment (replicates) of plots per site (see Supporting Information Fig. S1)
column I-LW	Plant abundance per species (in total 327 plant species) expressed as cover percentage estimation according to van der Maarel (vdM 1979; 7 classes: 1-7); nomenclature according to Lauber & Wagner (1996)

en: Fungi data

en:
Sample.data
Plot.ID	consecutive numbers for plots (in total 36 plots)
Treatment	One restoration treatment and two reference treatments. Topsoil+Propagules= Topsoil removal (upper 10-30 cm) combined with introduction of target plant species; Initial=intensively managed grasslands; Target= species-rich semi-wet to semi-dry grasslands
treat.yr	Treatment abbreviation. For restored grasslands: Treatment abbreviation + time since restoration; Initial + Target = NA
yr.trt	year when topsoil was removed; Initial + Target = NA
Age	time since restoration (sampling year 2018 - yr.trt); Initial + Target = NA
Age.class	restored sites of similar age grouped into four age classes. Y.4 = Year 3+4 (recently restored); Y.18 = Year 17+19 (mid-term); Y.24 = Year 23+25 (long-term); Y.30 = Year 27+32 (long-term); Initial + Target = NA
Cluster	clustered spatial arrangment of sites in the field (see Supporting Information Fig. S1)
Site	clustered spatial arrangment (replicates) of plots per site (see Supporting Information Fig. S1)

Taxonomy
OTU.ID	consecutive numbers for operational taxonomic units (OTUe 1-7794)
Taxonomic rank	Domain, Phylum, Class, Order, Family, Genus, Species

Abundance
columns	Plot.ID (see Sample.data)
rows	OTU.ID (see Taxonomy)

en:
This dataset contains all data, on which the following publication below is based.

Paper Citation:

_Resch, M.C., Schütz, M., Ochoa-Hueso, R., Buchmann, N., Frey, B., Graf, U., van der Putten, W.H., Zimmermann, S., Risch, A.C. (in review). Long-term recovery of above- and belowground interactions in restored grassland after topsoil removal and seed addition. Journal of Applied Ecology_

Please cite this paper together with the citation for the datafile.

Study area and experimental design
The study was conducted in and around two nature reserves, Eigental and Altläufe der Glatt, which were located approximately 5 km apart (47°27´ to 47°29´ N, 8°37´ to 8°32´ E, 417 to 572 m a.s.l., Canton of Zurich, Switzerland; Figure S1 and S2, Table S1). Mean annual temperature and precipitation are 9.8 ± 0.6 °C and 990 ± 168 mm (Kloten climate station 1988-2018; MeteoSchweiz, 2019). TFor this study, we used a space-for-time approach based on eight restoration sites that were between 3 and 32 years old. We measured recovery and restoration success by comparing the restored grasslands with intensively managed and semi-natural grasslands. Using a space-for-time approach requires high similarities in historical properties of the site, such as soil conditions and management regimes, to assure that temporal processes are appropriately represented by spatial patterns (Walker et al., 2010). This was the case in our study. The restored sites had similar soil conditions (i.e., soil type, structure, water availability) as the targeted semi-natural grasslands, while they shared the same agricultural legacy with intensively managed grasslands, i.e., biomass harvest and fertilization (manure and/or slurry) three to five times a year as well as tillage. We randomly established three 5 m x 5 m (25-m2) plots for plant identification and three 2 m x 2 m (4-m2) subplots for soil biotic and abiotic data collection at least 2 m away from the 25-m2 plots in each restoration site. Sites of similar age were grouped into four age classes: Y.4 (3 & 4 years after restoration), Y.18 (17 & 19 years), Y.24 (23 & 25 years), and Y.30 (27 & 32 years). Six intensively managed (Initial) and six semi-natural grassland (Target) sites complemented the experimental set-up, for a total of 36 plots. All plots were sampled under similar conditions, i.e., day of the year, air temperature, soil moisture, and time since last rain event, in June/July 2017 (intensively managed and semi-natural plots) and 2018 (restored plots).

Collection of plants and selected soil biota data
Plant species cover (in %) was visually estimated in each 25-m2 plot in mid-June (Braun-Blanquet, 1964; nomenclature: Lauber & Wagner, 1996). We calculated Shannon diversity and assessed plant community structure. We included soil microbial (fungi, procaryotes) and nematodes in our study as they represent the majority of soil biotic diversity and abundance (Bardgett & van der Putten, 2014), cover various trophic levels of the soil food web (Bongers & Ferris, 1999), and play key roles in soil functioning and ecosystem processes (Bardgett & van der Putten, 2014). In particular, soil nematodes were found to be well suited belowground indicators to evaluate recovery/development after restoration (e.g. Frouz, et al. 2008; Kardol et al., 2009; Resch et al., 2019). We randomly collected ten soil cores (2.2 cm diameter x 12 cm depths; sampler from Giddings Machine Company, Windsor, USA) in the 4-m2 subplots to assess soil nematode and microbial (fungal, prokaryotic) diversities and community structures. For soil nematodes, eight of the soil cores were combined and gently homogenized, placed in coolers and stored at 4 °C and transported to the laboratory (Netherlands Institute of Ecology, NIOO, Wageningen, Netherlands) within three days after collection. Free-living nematodes were extracted from 200 g of fresh soil using Oostenbrink elutriators (Oostenbrink, 1960). After extraction, each sample was divided into three subsamples, two for molecular identification and one to determine nematode abundance (see Resch et al., 2019). For the molecular work, two subsamples were stored in 70% ethanol (final volume 10 mL each) and transported to the laboratory at the Swiss Federal Research Institute WSL (Birmensdorf, Switzerland). Each subsample was reduced to roughly 200 μL by centrifugation and removal of the supernatant. The remaining ethanol was vaporized (65 °C for 3 h). Thereafter, 180 μL ATL buffer solution (Qiagen, Hilden, Germany) was immediately added and samples were stored at 4 °C until further processing. From these samples, nematode metagenomic DNA was extracted using the DNeasy Blood & Tissue Kit (Qiagen, Hilden, Germany) according to the manufacturer`s protocol, except for the incubation step which was run at 56 °C for 4 h. PCR amplification of the V6-V8 region of the eukaryotic small-subunit (18S) was performed with 7.5 μL of genomic DNA template (ca. 1 ng/μL) in 25 μL reactions containing 5 μL PCR reaction buffer, 2.5 mM MgCL2, 0.2 mM dNTPs, 0.8 μM of each primer (NemF: Sapkota & Nicolaisen, 2015; 18Sr2b: Porazinska et al., 2009), 0.5 μL BSA, and 0.25 μL GoTaq G2 Hot Start Polymerase (Promega Corporation, Madison, USA). Amplification was using an initial DNA denaturation step of 95 °C for 2 min, followed by 35 cycles at 94 °C for 40 sec, 58 °C for 40 sec, 72 °C for 1 min, and a final elongation step at 72 °C for 10 min. Filtering, dereplication, sample inference, chimera identification, and merging of paired-end reads was implemented using the DADA2 pipeline (v.1.12; Callahan et al., 2016) to finally assign amplicon sequence variants (ASVs) as taxonomic units.
We combined and homogenized the remaining two soil cores to assess soil microbes, placed them in coolers (4 °C) and transported them to the laboratory at WSL. Metagenomic DNA was extracted from 8 g sieved soil (2 mm) using the DNAeasy PowerMax Soil Kit (Qiagen, Hilden, Germany) according to the manufacturer´s protocol. PCR amplification of the V3-V4 region of the small-subunit (16S) of prokaryotes (i.e., bacteria and archaea) and the ribosomal internal transcribed spacer region (ITS2) of fungi was performed with 1 ng of template DNA using PCR primers and conditions as previously described (Frey et al., 2016). PCRs were run in triplicates, pooled and sent to the Genome Quebec Innovation Centre (Montreal, QC, Canada) for barcoding using the Fluidigm Access Array technology (Fluidigm) and paired-end sequencing on the Illumina MiSeq v3 platform (Illumina Inc., San Diego, USA). Quality filtering, clustering into operational taxonomic units (OTUs, 97% similarity cutoffs) and taxonomic assignment were performed as previously described (Resch et al., 2021).Taxonomic classification of nematode, prokaryotic and fungal sequences was conducted querying against the most recent versions of PR2 (v.4.11.1; Guillou et al., 2013), SILVA (v.132; Quast et al., 2013), and UNITE (v.8; Nilsson et al., 2019) reference sequence databases. Taxonomic assignment cutoffs were set to confidence rankings ≥ 0.8 (below ranked as unclassified). Prokaryotic OTUs assigned to mitochondria or chloroplasts as well as OTUs or ASVs assigned to other than Fungi or Nematoda were manually removed prior to data analysis. The three datasets were filtered to discard singletons and doubletons. Taxonomic abundance matrices were rarefied to the lowest number of sequences per community to achieve parity of the total number of reads between samples (Prokaryotes: 10,929 reads; Fungi: 18,337 reads; Nematodes: 6,662 reads). We calculated Shannon diversity and assessed community structures for soil nematodes, prokaryotes and fungi based on their relative abundances of ASV or OTU at the taxon level.

Collection of soil physical and chemical properties
We randomly collected one undisturbed soil core (5 cm diameter, 12 cm depth) per 4-m2 subplot using a steel cylinder that fit into the soil corer. The cylinders were capped to avoid disturbance during transport and used to measure field capacity, rock content and fine earth density as previously described (Resch et al., 2021). We randomly collected another three soil cores (5 cm diameter, 12 cm depths) in each 4-m2 subplot to determine soil chemical properties. The cores were pooled, dried at 60 °C for 48 h and passed through a 2 mm sieve. We measured soil pH (CaCl2) on dried samples, total nitrogen (N) and organic carbon (C) concentration on dried and fine-ground samples (≤ 0.5 mm; for details see Resch et al., 2021). We calculated total N and organic C pools after correcting its concentration for soil depth, rock content and fine earth density.

bacteria

display_name: bacteria

biodiversity

display_name: biodiversity

fungi

display_name: fungi

grassland

display_name: grassland

nematodes

display_name: nematodes

plants

display_name: plants

restoration

display_name: restoration

soil

display_name: soil

soil-biodiversity

display_name: soil-biodiversity

soil-biology

display_name: soil-biology

soil-chemistry

display_name: soil-chemistry

topsoil-removal

display_name: topsoil-removal

en: Long-term recovery of above-and belowground interactions in restored grasslands


en: lichens garten moose diversitat bryophytes flechten bryolich

en: Im Rahmen des Bryolich-Projekts “Moose und Flechten in Gärten” wurden möglichst vollständige Artenlisten von Moosen und Flechten in 26 bzw. 7 Gärten um Wohnhäuser erstellt. In 5 dieser Gärten wurden beide Artengruppen erfasst. Zusätzlich wurden Informationen über unterschiedliche Lebensräume innerhalb der Gärten (z.B. Fläche mit Gehölzen, Fläche von Blumenbeeten) und weitere Garten-Charakteristika (z.B. Fläche des Gartens, Alter des Gartens, Einsatz von Dünger) erfasst. Details zum Projekt und den erfassten Daten können im zugehörigen Artikel (Bergamini et al. 2024) und auf der Webseite von Bryolich gefunden werden (https://www.bryolich.ch/mfig/mfig_de.html).

bryolich

display_name: bryolich

bryophytes

display_name: bryophytes

diversitat

display_name: diversitat

flechten

display_name: flechten

garten

display_name: garten

lichens

display_name: lichens

moose

display_name: moose

educ

en: Education, culture and sport

envidat

en: EnviDat: the Environmental Data Portal

en: EnviDat is the WSL data portal providing unified and managed access to environmental monitoring and research data. The portal has the capability to host and publish data sets. Through the sharing of unique and high-value data sets worldwide, EnviDat fosters research and contributes to advancing environmental science.

en: Daten Bryolich-Projekt Moose und Flechten in Gärten


c-n-p-release-treeline

maintainer: Frank Hagedorn

title_for_slug: c-n-p-release-treeline

en: treeline-ecosystems biogeochemical-cycling litter-decomposition carbon-cycle microbial-biomass climate-change nutrient-fluxes enzymatic-activities

en: Litter layer characteristics, C-N-P-release during decomposition, microbial C-N-P, enzyme activity, mineralization of 13C-labeled glucose-6-phosphate from samples collected across two treelines

en:
1. Chemical characteristics of litter layer sampled along elevation gradient across treeline ecotones in the Khibiny mountains (birch) and South Urals (spruce)
2. Release of C-N-P during decomposition at 5°C and 15° studied in an incubation experiment with microlysimeters
3. Data on microbial biomass C-N-P, potential activity of C-N-P requiring enzymes in the litter layer
4. Mineralization of 13C labeled glucose-6 phosphate, microbial 13C uptake, and net P immobilization of released P to identify microbial processing of labile organic P

biogeochemical-cycling

display_name: biogeochemical-cycling

carbon-cycle

display_name: carbon-cycle

climate-change

display_name: climate-change

enzymatic-activities

display_name: enzymatic-activities

litter-decomposition

display_name: litter-decomposition

microbial-biomass

display_name: microbial-biomass

nutrient-fluxes

display_name: nutrient-fluxes

treeline-ecosystems

display_name: treeline-ecosystems

en: C-N-P-Release Treeline


en: forest climate-change biodiversity statistical-interpolation microclimate ecology radiation-transfer

media_type: application/zip

en: Predicted microclimate topsoil temperatures at 5 cm below ground. 10 m spatial resolution raster files are provided for mean daily minimum (tmin), mean (tmean) and maximum (tmax) temperatures during each month from April (04) to October (10) over the period between 2012 to 2021.

format: ZIP

en: Predicted microclimate air temperatures at 100 cm above ground. 10 m spatial resolution raster files are provided for mean daily minimum (tmin), mean (tmean) and maximum (tmax) temperatures during each month from April (04) to October (10) over the period between 2012 to 2021.

en: Predicted microclimate air temperatures at 5 cm above ground. 10 m spatial resolution raster files are provided for mean daily minimum (tmin), mean (tmean) and maximum (tmax) temperatures during each month from April (04) to October (10) over the period between 2012 to 2021.

en: Climate data matching the scales at which organisms experience climatic conditions are often missing. Yet, such data on microclimatic conditions are required to better understand climate-change impacts on biodiversity and ecosystem functioning. Here we combine a national network of microclimate temperature measurements with a novel radiative transfer model to map monthly minimum, mean and maximum temperatures during the vegetation period at a 10 meter spatial resolution across Switzerland. The temperature measurements took place in 107 sampling plots distributed across different habitat types, with 62 plots in forests, 22 below trees outside forests, and 23 in open grasslands. In each plot we measured temperature in the topsoil (-5cm), as well as in the air at 5cm and 100cm height above ground. Spatial interpolation was achieved by using a hybrid approach based on linear mixed effects models with input from detailed radiation estimates that account for topographic and vegetation shading, as well as other predictor variables related to the macroclimate, topography and vegetation height. Our data reveals strong horizontal and vertical variability in microclimate temperature, particularly for maximum temperatures at 5 cm above the ground and within the topsoil. Compared to macroclimate conditions as measured by weather stations outside forests, diurnal air and topsoil temperature ranges inside forests were reduced by up to 3.0 and 7.8 °C, respectively, while below trees outside forests, e.g. in hedges and below solitary trees, this buffering effect was 1.8 and 7.2 °C. We also found that in open grasslands, maximum temperatures at 5 cm above ground are on average 3.4 °C warmer than that of macroclimate, suggesting that in such habitats heat exposure close to the ground is often underestimated when using macroclimatic data. After accounting for macroclimate effects, microclimate patterns were primarily driven by radiation, with particularly strong effects on maximum temperatures. Results from spatial block cross-validation revealed predictive accuracies as measured by RSME’s ranging from 1.18 to 3.43 °C, with minimum temperatures generally being predicted more accurately than maximum temperatures. The microclimate maps presented here enable a more biologically relevant perspective when analysing climate-species interactions, which is expected to lead to a better understanding of biotic and ecosystem responses to climate and land use change.

biodiversity

display_name: biodiversity

ecology

display_name: ecology

forest

display_name: forest

microclimate

display_name: microclimate

radiation-transfer

display_name: radiation-transfer

statistical-interpolation

display_name: statistical-interpolation

en: Monthly topsoil and near surface microclimate temperature data for Switzerland


maintainer: Elisabeth Hafner

en: satellite natural-hazard hazard-mapping avalanche snow

en: SPOT6 Avalanche Outlines 16 January 2019

en: Shapefile of the manually mapped avalanche outlines. Please only use this data together with the example key document provided with this dataset and within the limitations of the dataset described in the publications.

format: SHP

en:
Outlines of 6'041 avalanches mapped from SPOT6 satellite data over the Swiss Alps on 16 January 2019. The dataset was acquired following a period with very high avalanche danger. The outlines have different attributes described in the data example key (ExampleKey_AvalMapping16012019.pdf)

The generation of the data is described in:

Bühler, Y., E. D. Hafner, B. Zweifel, M. Zesiger, and H. Heisig (2019), Where are the avalanches? Rapid SPOT6 satellite data acquisition to map an extreme avalanche period over the Swiss Alps, The Cryosphere, 13(12), 3225-3238, doi:10.5194/tc-13-3225-2019.

The data was comprehensivly validated in a subset area in

Hafner, E.D.; Techel, F.; Leinss, S.; Bühler, Y., 2021: Mapping avalanches with satellites - evaluation of performance and completeness. Cryosphere, 15, 2: 983-1004. doi: 10.5194/tc-15-983-2021

avalanche

display_name: avalanche

hazard-mapping

display_name: hazard-mapping

natural-hazard

display_name: natural-hazard

satellite

display_name: satellite

snow

display_name: snow

en: SPOT6 Avalanche outlines 16 January 2019


en: soil-solution forest-ecosystems xylem-water water-isotopes water-budget

media_type: image/png

en: Overview of most deposition water isotopic signatures.

format: PNG

en: Overview of most bulk soil water isotopic signatures.

en: Water isotope signatures and gravimetric water content of xylem samples.

en: Column descriptions for soil solution, deposition, xylem and bulk soil samples.

en: Overview of most soil solution water isotopic signatures.

en: Water isotopic signature of deposition samples.

en: Water isotope signatures of soil solution samples.

en: Water isotope signatures and gravimetric water content of bulk soil samples.

en: Overview of most xylem water isotopic signatures.

en:
The isotope composition of different forest water pools was analyzed at 10 sites of the Long-term Forest Ecosystem Research programme in 2021 and 2022. The sampling was done during the vegetation season and included fortnightly xylem water samples taken by stem increment cores and each year 3 bulk soil water sampling campaigns (in April, June, September of 2021 and 2022). Both sample types were cryogenically extracted at WSL and analyzed on a Picarro 2140 with Micro-Combustion-Module. Gravimetric water content in both sample types was computed based on pre-and post-extraction weights. In addition to xylem and bulk soil waters, we analyzed the isotope composition of soil solution from a suction cup lysimeters in three soil depths 0, 15, 50, 80 cm and precipitation from samplers below the canopy and outside of the forest, all collected fortnightly from collection periods of varying length (longest from 2017-2022).
Precipitation samples are further described [here](https://www.doi.org/10.16904/envidat.lwf.15). Lysimeter samples are described further [here](https://www.doi.org/10.16904/envidat.lwf.28).

forest-ecosystems

display_name: forest-ecosystems

soil-solution

display_name: soil-solution

water-budget

display_name: water-budget

water-isotopes

display_name: water-isotopes

xylem-water

display_name: xylem-water

educ

en: Education, culture and sport

envidat

en: EnviDat: the Environmental Data Portal

en: EnviDat is the WSL data portal providing unified and managed access to environmental monitoring and research data. The portal has the capability to host and publish data sets. Through the sharing of unique and high-value data sets worldwide, EnviDat fosters research and contributes to advancing environmental science.

en: Water isotope signatures in Swiss forest ecosystems in 2021 and 2022


en: environmental---history historical-carthography wetlands environmental--policy switzerland ecology

en: Wetlands 1850 - 2010 (shapefiles)

en:
 History of wetlands - GIS-Layers
 Location of wetlands based on signatures in topographic maps
* Basis 1850: original measuring table sheets Dufour created between the years 1834 and 1863.
* Basis 1900/ Basis 1950: The Siegfried maps were updated and published at regular intervals between 1870 and 1949. This long period of time made it possible to reconstruct wetlands for two periods based on the Siegfried Maps: the first edition (hereinafter referred to as "1900") and the last edition ("1950").
* Basis 2010: Map sheets from the National Map from 2006 to 2011 were used for the most recent time period of the reconstruction.
 Location of wetlands due to reconstructions
The reconstruction **must not** be interpreted in the sense of a surface-accurate separation, but shows without claim to location accuracy the approximate extent of the areas that would have corresponded to the mapping criteria for wetlands used in today's topographic maps around 1850, 1900 and 1950. The basics can be found in Stuber & Bürgi 2019, chapter 5.4.

mimetype: application/zip

en:
Naturally, large parts of the Swiss Plateau are characterised by wetlands
and meandering rivers. That this is no longer the case today is the result
of centuries of efforts to obtain dry land. But how did this process take
place? What were the relevant actors and what were their motivations? And
what can be said about the ecological consequences of this development?

In a research project on the history of wetlands in Switzerland since 1700,
we conducted (a) a historical analysis of the development of land use in
wetlands and the actors involved, (b) a historical-cartographic
reconstruction of wetland extent since 1850 and (c) an evaluation of
ecological effects of changes in wetlands on various organisms groups.

The series of GIS layers on wetland history stem from the second part of
the project. The area reconstruction is based on digitized and homogenized
signatures from national map series, as they have been available since
about 1850. Details about the digitalization process and the homogenization
procedures applied ("Rekonstruktionen") are included in Stuber & Bürgi
2019.

Book Citation:
 > Stuber M, Bürgi M (2019) Vom «eroberten Land» zum Renaturierungsprojekt. Geschichte der Feuchtgebiete in der Schweiz seit 1700. "Bristol Schriftenreihe", Band 59. Haupt Verlag, Bern, Stuttgart, Wien. 262 Seiten.

environmental---history

display_name: environmental---history

environmental--policy

display_name: environmental--policy

historical-carthography

display_name: historical-carthography

switzerland

display_name: switzerland

wetlands

display_name: wetlands

en: History of wetlands in Switzerland since 1850


tree-species-map-of-switzerland

maintainer: Tiziana Li Koch

title_for_slug: tree-species-map-of-switzerland

en: map remote-sensing tree-species forest switzerland

en: Image of the tree species map

en:
Dominant tree species map of Switzerland
We created a tree species map of Switzerland for the dominant tree species in the forested areas. The spatial resolution of the map is 10 m and the coordinate system is ETRS89-extended / LAEA Europe (EPSG 3035). The map comprises Sentinel-2 index time series from the year 2020, a digital elevation model and species reference data from the Swiss National Forest Inventory. The map is available as raster (.tif) or vector dataset (.gpkg).
**Access will be granted upon request.**
In total, the following 15 species were mapped:
*Abies alba*, *Acer pseudoplatanus*, *Alnus glutinosa*, *Alnus incana*, *Betula pendula*, *Castanea sativa*, *Fagus sylvatica*, *Fraxinus excelsior*, *Picea abies*, *Pinus cembra*, *Pinus mugo arborea*, *Pinus sylvestris*, *Quercus petraea*, *Quercus robur*, *Sorbus aucuparia*.

 Approach

 Data
- Swiss National Forest Inventory Data (stand species with > 60 % dominance in upper canopy; on at least more than 9 plots dominant)
- Sentinel-2 time series (2020, Indices: CCI, CIRE, NDMI, EVI, NDVI)
- Digital elevation model (DEM) (swissalti3d, 5 m)
- Biogeographical regions (Federal Office for the Environment FOEN)
- Forest mask 2017 (Approach: Waser et al., 2015)

 Modeling approach
We identified the most meaningful variables that led to separation of the respective groups by using random forest models with a forward feature selection (Meyer et al., 2018; Ververidis & Kotropoulos, 2005). In this approach, the final random forest model is solely built from the selected meaningful variables. By identifying meaningful variables, we can determine which variables might influence the grouping. Further, to avoid overfitting and overly optimistic results, we applied 10-fold spatial cross-validation and put all pixels from a plot in the same spatial fold.
The modeling was realized using the CAST package in R (Meyer et al., 2022), based on the well-known caret package (Kuhn, 2022). We used the ranger package in R (Wright & Ziegler, 2017) to implement the random forest models, due to its short computation time.

 Training data for modeling
- 295 Sentinel-2, DEM & Biogeographical variables
- 10525 tree species pixels

 Selected variables for final model
1. EVI of 2020.05.16
2. NDMI of 2020.03.12
3. CIRE of 2020.04.16
4. NDMI of 2020.07.05
5. CCI of 2020.05.11
6. dem
7. CCI of 2020.08.14
8. NDMI of 2020.08.24
9. CCI of 2020.12.22
10. NDMI of 2020.04.21
11. NDMI of 2020.11.17
12. NDMI of 2020.08.09
13. CIRE of 2020.03.22
14. CIRE of 2020.08.09
14. CCI of 2020.11.02
15. CIRE of 2020.06.10

 Overall Accuracy of final model
- 0.759

 Nationwide prediction
- Predicted throughout forest mask 2017 (Approach: Waser et al., 2015)
- Not applied on incomplete Sentinel-2 time series (own category in final map: incomplete_ts)
- Applied the Area of Applicability (Meyer 2022) to sort out pixels outside of the feature space; basically where the model had not the same values for pixels as in the available training data

 *Be aware that the map is only validated with the training data itself, an independent validation with other data sources remains missing*

 References
- Kuhn, M. (2022). Classification and Regression Training. 6.0-93.
- Meyer, H., Reudenbach, C., Hengl, T., Katurji, M., & Nauss, T. (2018). *Improving performance of spatio-temporal machine learning models using forward feature selection and target-oriented validation*. Environmental Modelling and Software, 101, 1-9. https://doi.org/10.1016/j.envsoft.2017.12.001
- Meyer, H., Milà, C., & Ludwig, M. (2022). *CAST: 'caret' Applications for Spatial-Temporal Models*. 0.7.0.
- Ververidis, D., & Kotropoulos, C. (2005). *Sequential forward feature selection with low computational cost*. 2005 13th European Signal Processing Conference.
- Waser, L., Fischer, C.,Wang, Z., & Ginzler, C. (2015). *Wall-to-Wall Forest Mapping Based on Digital Surface Models from Image-Based Point Clouds and a NFI Forest Definition*. Forests, 6, 12, 4510–4528.
- Wright, M. N., & Ziegler, A. (2017). *ranger: A Fast Implementation of Random Forests for High Dimensional Data in C++ and R*. Journal of Statistical Software, 77(1), 1-17. https://doi.org/doi:10.18637/jss.v077.i01

forest

display_name: forest

map

display_name: map

remote-sensing

display_name: remote-sensing

tree-species

display_name: tree-species

en: Tree species map of Switzerland


en: biological-control multilocus-genotypes simple-sequence-repeats switzerland population-genetics nuclear-microsatellite-markers trichopria-drosophilae drosophila-suzukii

en: Table comprising all pertinent information for multiplex PCRs of species-specific nuclear microsatellite makers for Trichopria drosophilae, comprising all 21 newly developed markers, details on full sequences with GenBank accession numbers, primer sequences (including labeling and pig-tails), and repeat motives. PCRs with respective annealing temperatures (AnnealingTemp) refer to Type-It Multiplex PCR Kit (Qiagen, Hilden, Germany).

mimetype: text/csv

en: Multilocus genotypes (biallelic coding for 21 nuclear microsatellites) of Trichopria drosophilae described in Gugerli et al. Agrarforschung Schweiz 2019. Missing data denoted as '999'. Population codes (PopNo) are the following: 1, Vezia; 3, Contone ; 5, Davesco; 6, Corteglia; 7, Mezzana; 8, Stabio; 9, Gordola; 10, Sementina; 12, Brusata di Novazzano; 14, Monteggio; 16, Giubiasco; 17, ComoBP; 18, VD; 19, Weil_D; 20, Dossenheim; 21, BioPlanet_Como. Coordinates (CoordCH_E, CoordCH_N) refer to the Swiss coordinates system CH1903.

en:
 Nuclear microsatellite markers and genotype data for _Trichopria ddrosophilae_

This data set comprises (i) the characteristics of a set of 21 species-specific nuclear microsatellites for PCR amplification in _Trichopria drosophilae_ (ii) and genotype data for samples collected in southern Switzerland (Canton of Ticino), with few reference samples from Canton of Vaud, southern Germany, and northern Italy (lab-reared population).
Markers were developed by Ecogenics GmbH, Balgach (Switzerland), using MiSeq Nano 2x250 v2 format (on a mix of 10 individuals). Multiplex PCR assays for multilocus genotyping were established by Ecological Genetics (WSL Birmensdorf), and population genetic analyses are found in Gugerli et al., Agrarforschung Schweiz 2019.

biological-control

display_name: biological-control

drosophila-suzukii

display_name: drosophila-suzukii

multilocus-genotypes

display_name: multilocus-genotypes

nuclear-microsatellite-markers

display_name: nuclear-microsatellite-markers

population-genetics

display_name: population-genetics

simple-sequence-repeats

display_name: simple-sequence-repeats

trichopria-drosophilae

display_name: trichopria-drosophilae

en: Nuclear microsatellite markers for Trichopria drosophilae, parasitoid wasp on Drosophila suzukii


maintainer: Izabela Bujak-Ozga

en: drainage-network catchment dataset channel erlenbach catchment-data precipitation drainage dynamics water-level data

en: The dataset contains time series of water levels, precipitation measured in the two sub-catchments of the Erlenbach catchment and its vicinity during summer and autumn 2021, as well as flowing drainage network lengths calculated for these areas using the CEASE method developed by the authors. Detailed description of the dataset is provided in the documentation.

catchment

display_name: catchment

catchment-data

display_name: catchment-data

channel

display_name: channel

data

display_name: data

dataset

display_name: dataset

drainage

display_name: drainage

drainage-network

display_name: drainage-network

dynamics

display_name: dynamics

erlenbach

display_name: erlenbach

precipitation

display_name: precipitation

water-level

display_name: water-level

educ

en: Education, culture and sport

envidat

en: EnviDat: the Environmental Data Portal

en: Short-term Drainage Density Dynamics Dataset for the Erlenbach Catchment


data-konzeptionelles-systemmodell

maintainer: Matthias Bürgi

title_for_slug: data-konzeptionelles-systemmodell

en: landscape-change scenarios climate-change policy-action qualitative-research

en:
This folder contains documents relevant to the project step Konzeptionelles Systemmodell. It specifically contains the following documents:

1. 0201_Konzeptionelles Systemmodell_20221027: This document is the final version of the Konzeptionelles Systemmodell. The underlying structure of the Konzeptionelles Systemmodell is explained in chapter 4.4 of the document 0202_Masterarbeit Elena Siegrist_UniBern_Herbstsemester 2022 also deposited in this folder. The document contains 3 sheets. The sheet "Bausteine" shows the different possible options for table columns of the type Bausteine (see chapter 4.4 of Masterarbeit), the sheet "Direkte Effekte" contains identified direct impact pathways and the sheet "Indirekte Effekte" contains identified indirect impact pathways.

2. 0202_Masterarbeit Elena Siegrist_UniBern_Herbstsemester 2022: This document is the Master Thesis of Elena Grace Siegrist submitted to and accepted by the University of Bern in the Autumn Semester 2022. Chapter 4.4 of the document explains the underlying structure of the Konzeptionelles Systemmodell.

3. 0203_Literaturverzeichnis_konzeptionelles Systemmodell_20221026: This document lists all literature and documents cited in the Konzeptionelle Systemmodell.

climate-change

display_name: climate-change

landscape-change

display_name: landscape-change

policy-action

display_name: policy-action

qualitative-research

display_name: qualitative-research

scenarios

display_name: scenarios

en: EnviDat is the WSL data portal providing unified and managed access to environmental monitoring and research data. The portal has the capability to host and publish data sets. Through the sharing of unique and high-value data sets worldwide, EnviDat fosters research and contributes to advancing environmental science.

en: Data Konzeptionelles Systemmodell


en: precipitation solar-radiation growing-degree-days temperature relative-humidity soil-water-balance growing-season-length

en: CHELSA-BIOCLIM+

en: Global extented set of bioclimatic variables at different temporal (e.g. monthly, annual, long term normals) resolution in Geotiff format.

en: CHELSA-BIOCLIM+ Technical Documentation

en: Technical documentation document including the variable names, units, scaling, offset, and background.

en: A multitude of physical and biological processes on which ecosystems and human societies depend are governed by climatic conditions. Understanding how these processes are altered by climate change is central to mitigation efforts. Based on mechanistically downscaled climate data, we developed a set of climate-related variables at yet unprecedented spatiotemporal detail as a basis for environmental and ecological analyses. We created gridded data for near-surface relative humidity (hurs), cloud area fraction (clt), near-surface wind speed (sfcWind), vapour pressure deficit (vpd), surface downwelling shortwave radiation (rsds), potential evapotranspiration (pet), climate moisture index (cmi), and site water balance (swb), at a monthly temporal and 30 arcsec spatial resolution globally starting 1980 until 2018. At the same spatial resolution, we further estimated climatological normals of frost change frequency (fcf), snow cover days (scd), potential net primary productivity (npp), growing degree days (gdd), and growing season characteristics for the periods 1981-2010, 2011-2040, 2041-2070, and 2071-2100, considering three shared socioeconomic pathways (SSP126, SSP370, SSP585) and five Earth system models. Time-series variables showed high accuracy when validated against observations from meteorological stations. Climatological normals were also highly correlated to observations although some variables showed notable biases, e.g., snow cover days (scd). Together, the data sets presented here allow improving our understanding of patterns and processes that are governed by climate, including the impact of recent and future climate changes on the world’s ecosystems and associated services to societies.

growing-degree-days

display_name: growing-degree-days

growing-season-length

display_name: growing-season-length

relative-humidity

display_name: relative-humidity

soil-water-balance

display_name: soil-water-balance

solar-radiation

display_name: solar-radiation

temperature

display_name: temperature

en: CHELSA-BIOCLIM+ A novel set of global climate-related predictors at kilometre-resolution


carabid-beetles-in-forests

maintainer: Martin K. Obrist

title_for_slug: carabid-beetles-in-forests

en: carabidae trapping insects running-beetles arthropoda forest coleoptera

en: Tab-delimited data of the according sql query.

en: Data query used on Fauna Database to retrieve the submitted data.

en: SQL query used to extract the data from fauna database.

en: Data extract in TAB-delimted format. First row is header, first column is counter.

en:
Carabidae data from all historic up to the recent projects (21.10.2019) of WSL, collected with various methods in forests of different types.

Version 2 ('FIDO_global_extract 2019-11-22_18-11-24 WSL-Forest-Carabidae') contains additional data field PROJ_FALLENBEZEICHNUNG.

Data are provided on request to contact person against bilateral agreement.

arthropoda

display_name: arthropoda

carabidae

display_name: carabidae

coleoptera

display_name: coleoptera

forest

display_name: forest

insects

display_name: insects

running-beetles

display_name: running-beetles

trapping

display_name: trapping

en: Carabid beetles in forests


en: qpcr environmental-dna edna threatened-species field-based-protocol biodiversity-monitoring crispr-dx crispr-cas african-manatee

en: Description of project and folders and files

en:
Folder containing the data files with Cp values (qPCR) and the CRISPR-Dx classifications. CRISPR_field_based_classifications.csv file contains the classifications per pool per extract (0: no detection, 1: detection) for the African manatee (Trichechus senegalensis).
CRISPR_lab_based_classifications.csv file contains the classifications per pool per extract (0: no detection, 1: detection).
qPCR_Cp_2nd_derivative.csv file contains the Cp value of the 8 replicates of each extract.

en: File containing overview of site names and extract number (field-based or lab-based extraction). The extract_number_field_based corresponds to the identically called column in CRISPR_field_based_classifications.csv file in the data folder, as the extract_number_lab_based to the column in the file CRISPR_lab_based_classifications.csv file and the qPCR_Cp_2nd_derivative.csv file (also in the data folder). The file includes the GPS coordinates of the sampling location (transect start point).

en:
Data associated to the publication "Rapid field-based detection of a threatened and elusive species with environmental DNA and CRISPR-Dx"

 Authors:

Flurin Leugger, Martina Lüthi, Michel Schmidlin, Zacharias Kontarakis and Loïc Pellissier

 Contact:

flurinleugger@gmail.com
loic.pellissier@usys.ethz.ch

 Project description:

We collected eDNA samples in the Conkouati-Douli National Park in the Republic of Congo in 2023 in collaboration with Beauval Nature and HELP Congo. We analyzed the samples on site in the national park using CRISPR-Dx assays to detect the African manatee (*Trichechus senegalensis*). Additionally, we transported the remaining samples (buffer) to Switzerland and used a high-sensitivity protocol with CRISPR-Dx assays and a qPCR assay to verify the field-based detections. The qPCR of Hunter et al. (2018) detects the genus manatee (Trichechus). See publication for more details (doi will be added after publication).

 Folders:

 lateral_flow_tests_images\:

Images of the lateral flow tests used to analyze the eDNA extracts in the national park. File names correspond to the site names. At each site, we took two filter replicates. We ran 8 PCRs per filter/extract and pooled two PCRs together, resulting in 4 CRISPR-Dx assays per extract. The EVE number on top of the tests indicates the environmental extract number we use to track the extracts in our data base. It corresponds to the extract_number_field_based in the metadata and data folder. The negative extraction control with the strongest "band" was placed right to the eDNA extract on each image (labelled hand written with NC x.y).

 metadata\:

File containing overview of site names and extract number (field-based or lab-based extraction). The extract_number_field_based corresponds to the identically called column in CRISPR_field_based_classifications.csv file, as the extract_number_lab_based to the column in the file CRISPR_lab_based_classifications.csv file and the qPCR_Cp_2nd_derivative.csv file. The file includes the GPS coordinates of the sampling location (transect start point).

 data\:

Folder containing the files with Cp values (qPCR) and the CRISPR-Dx classifications. CRISPR_field_based_classifications.csv file contains the classifications per pool per extract (0: no detection, 1: detection) for the African manatee (Trichechus senegalensis).
CRISPR_lab_based_classifications.csv file contains the classifications per pool per extract (0: no detection, 1: detection).
qPCR_Cp_2nd_derivative.csv file contains the Cp value of the 8 replicates of each extract.

african-manatee

display_name: african-manatee

biodiversity-monitoring

display_name: biodiversity-monitoring

crispr-cas

display_name: crispr-cas

crispr-dx

display_name: crispr-dx

edna

display_name: edna

environmental-dna

display_name: environmental-dna

field-based-protocol

display_name: field-based-protocol

qpcr

display_name: qpcr

threatened-species

display_name: threatened-species

educ

en: Education, culture and sport

envidat

en: EnviDat: the Environmental Data Portal

en: Field-based eDNA analysis to detect the threatened and elusive African manatee


maintainer: Anita C. Risch

en: climate soil nitrogen fertilization global-change nutrient-network nitrification grassland mineralization ammonification herbivore

en: Risch et al. 2020 - Raw data for publication "Global impacts of fertilization and herbivore removal on soil net nitrogen mineralization are modulated by local climate and soil properties"

en:
we assessed how the removal of mammalian herbivores (Fence) and fertilization with growth-limiting nutrients (N, P, K, plus nine essential macro- and micronutrients; NPK) individually, and in combination (NPK+Fence), affected potential and realized soil net Nmin across 22 natural and semi-natural grasslands on five continents. Our sites spanned a comprehensive range of climatic and edaphic conditions found across the grassland biome. We focused on grasslands, because they cover 40-50% of the ice-free land surface and provide vital ecosystem functions and services. They are particularly important for forage production and C sequestration. Worldwide, grasslands store approximately 20-30% of the Earth’s terrestrial C, most of it in the soil (Schimel, 1995; White et al., 2000).

Study sites and experimental design
The 22 sites contributing to this project are part of the Nutrient Network Global Research Cooperative (NutNet, https://nutnet.umn.edu/). Mean annual temperature across our 22 sites ranged from -4 to 22°C, mean annual precipitation from 252 to 1,592 mm, and elevations from 6 to 4,261 m above sea level (Fig. 1, Supplementary Table S1). Soil organic C varied from 0.8 to 7.8%, soil total N from 0.1 to 0.6%, and the soil C:N ratio from 9.1 to 21.5. Soil clay content spanned from 3.0 to 35%, and soil pH from 3.4 to 7.6 (Supplementary Table S2). Thus, the sites covered a wide range of environments in which grasslands occur (Fig. 1, Supplementary Table S1 & S2).
At each site, the effects of nutrient addition and herbivore removal were tested via a randomized-block design (Borer et al., 2014; Supplementary Fig. S1a). Three replicate blocks with 10 treatment plots each were established at each site, with the exception of the site at bldr.us, where only two blocks were established (Supplementary Fig. S1a). The 10 plots were randomly assigned to a nutrient or fencing treatment, but only a subset of four plots was used in the current study, each with a different treatment (see below; Supplementary Fig. S1a). All plots were 5 x 5 m and divided into four 2.5 x 2.5 m subplots (Supplementary Fig. S1b). Each subplot was further divided into four 1 x 1 m square sampling plots, one of which was set aside for soil sampling (Borer et al., 2014; Supplementary Fig. S1b). Plots were separated by at least 1 m wide walkways.
In this study, we collected data from the following four treatments: (i) untreated control plots (Control), (ii) herbivore removal plots (Fence), (iii) plots fertilized with N, P, K, plus nine essential macro and micronutrients (NPK), and (iv) plots with simultaneous fertilizer addition and herbivore removal (NPK+Fence; Supplementary Fig. S1a). The number of years of treatment differed among sites (2 – 9 years since start of treatment; Supplementary Table S1). For the nutrient additions, all sites applied 10 g N m-2 yr-1 as time-release urea; 10 g P m-2 yr-1 as triple-super phosphate; 10 g K m-2 yr-1 as potassium sulfate. A micro-nutrient mix (Fe, S, Mg, Mn, Cu, Zn, B, Mo, Ca) was applied at 100 g m-2 together with K in the first year of treatments but not thereafter.
The vertebrate herbivore removal treatment (Fence) was established by fencing two plots, one control and one NPK plot, within each of the blocks (Supplementary Fig. S1a). We designed the fences so that they would effectively exclude aboveground mammalian herbivores with a body mass of over 50 g (Borer et al., 2014). At the majority of sites, the height of the fences was 180 cm, and the fence design included wire mesh (1 cm holes) on the first 90 cm along with a 30 cm outward-facing flange stapled to the ground to exclude burrowing animals; climbing and subterranean animals may potentially still access these plots (Borer et al., 2014). For slight modifications in fence design at a few sites see Supplementary Table S3. While most sites only had native herbivores, a few sites (4) were also grazed by domestic animals (Supplementary Table S1).
Potential and realized soil net N mineralization, ammonification, nitrification and other soil properties
Each site participating in the study received a package containing identical material from the Swiss Federal Institute for Forest, Snow and Landscape Research (WSL) to be used for sampling and on-site N incubations. For the field incubation, we followed the protocol by Risch et al. (2015, 2019). Briefly, we drove a 5 x 15 cm (diameter x depth) steel cylinder 13.5 cm deep into the soil after clipping the vegetation at randomized locations in each plot. The top 1.5 cm of the cylinder remained empty to capture incoming N from run-off or deposition with a polyester mesh bag (mesh-size 250 µm) filled with 13.2 ± 0.9 g of acidic and alkaline exchanger resin (1:1 mixture; ion-exchanger I KA/ion-exchanger III AA, Merck AG, Darmstadt). The bag was fixed in place with a metal Seeger ring (Bruetsch-Rüegger Holding, Urdorf, Switzerland). We then removed 1.5 cm soil at the bottom of the cylinder and placed another resin bag to capture N leached from the soil column. The exchange resin was saturated with H+ and Cl- prior to filling the bags by stirring the mixture in 1.2M HCl for 1 h and then rinsing it with demineralized water until the electrical conductivity of the water reached 5 μS/cm. The cylinders were then re-inserted into the cored hole, level with the soil surface, and incubated for an average of 42 days (range 40 to 57days). The individual site coordinators chose the timing of incubation to start approximately six weeks prior to peak plant biomass production. All incubations were completed between February 2015 and January 2016 accounting for differences in growing season between northern and southern hemispheres. At the end of the incubation, the cylinders were re-collected and immediately shipped to WSL in an insulated box together with cold packs to halt further mineralization. Gloves were worn at all times to avoid contamination of the samples. Upon arrival at WSL, we extracted the resin bags and a 20 g subsample of sieved soil (4 mm) separately in a 100 ml PE-bottle with 80 ml 1 M KCl for 1.5 h on an end-over-end shaker and filtered through ashless folded filter paper (DF 5895 150, ALBET LabScience). We measured NO3- (colorimetrically; Norman & Stucki, 1981) and NH4+concentrations (flow injection analysis; FIAS 300, Perkin Elmer) on these filtrates.
At the start of the field incubation, we additionally collected two soil cores of 5 x 12 cm (diameter x depth) in each sampling plot and composited them to measure potential soil net Nmin, soil chemical and biological properties (see below). We also collected an additional sample (5 x 12 cm) to assess soil physical properties, which remained within the steel cylinder. Both ends were tightly closed with plastic caps. Cores were carefully packed to avoid further disturbance, and together with the composited soil samples, were shipped to the laboratory at WSL within a few days after collection.
From the composited samples, we extracted an equivalent of 20 g dry soil with KCl, as described above, and measured NO3- and NH4+concentrations. Realized soil net Nmin was then calculated as the difference between the inorganic N content of samples collected at the end of the incubation (plus N extracted from the bottom resin bag) and the N content at the beginning of the incubation; values were scaled to represent daily mineralization rates (mg N kg-1soil d-1; Risch et al., 2015). Realized soil net Nmin values represent an average period of 42 days prior to peak biomass, typically the highest period of biological activity, and not the entire year (Risch et al., 2019).
A second subsample of the composited sample was used to determine potential soil net Nmin in the laboratory (Risch et al., 2019). Briefly, we weighed duplicate samples (8 g dry soil) into 50-ml Falcon tubes. Soil moisture was brought to 60% of the field capacity of each plot, the Falcon tubes tightly closed and then incubated at 20°C for 42 days in a dark room. Every week the Falcon tubes were opened and ventilated. At the end of the incubation, the soil samples were extracted the same way as described above and NO3- and NH4+ was determined. Potential soil net Nmin was calculated as the difference between the N content before and after the incubation and scaled to represent daily values (mg N kg-1soil d-1). Using our NO3- and NH4+ measures we also calculated potential and realized soil net nitrification and soil net ammonification to be able to better understand the drivers of fertilization and herbivore removal effects on potential and realized soil net Nmin.
A third subsample of the composite soil sample was sieved (2 mm mesh) and microbial biomass (μg Cmic g-1 soil dry weight) was estimated by measuring the maximal respiratory response to the addition of glucose solution (4 mg glucose per g soil dry weight dissolved in distilled water; substrate-induced respiration method) on approximately 5.5 g of soil (Anderson & Domsch, 1978). The rest of the composited sample was dried at 65°C for 48 h, ground and sieved (2 mm mesh) to assess a series of soil chemical properties (Risch et al., 2019). We measured the percentage of clay as an indicator of soil texture (Gee & Bauder, 1986; Risch et al., 2019).
Statistical analyses
Potential and realized soil net Nmin were square root transformed to account for a highly skewed data distribution (yt = sign(y)*sqrt|y|; negative values in the data set impeded log transformation). To assess treatment effects on potential and realized soil net Nmin, we used linear mixed effects models (LMMs) fitted by maximum likelihood using the lme function from the nlme package (version 3.131.1; Pinheiro et al., 2016), R version 3.6.1; R Foundation for Statistical Computing. Treatment (Control, Fence, NPK, NPK+Fence) was a fixed factor, with site and block as random factors, where block was nested within site. We also tested for effects of time since start of treatments in preliminary analyses by adding total treatment years as an additional fixed factor. We did not find a significant effect of years of treatment, and thus dropped this variable from the models. The LMMs were corrected using varIdent if the homogeneity of variance criterion was not met (Pinheiro et al., 2016). To visualize our results, we calculated treatment effects using Cohens’ d statistic (Cohen, 1977; Koricheva et al., 2013). Note that calculating response ratios (or log response ratios) was not possible with our data, as we have both negative and positive values. We also fitted LMMs for potential and realized soil net ammonification and nitrification to gain more insight into how global change affects the processes underpinning potential and realized soil net Nmin. We also sqrt-transformed (see above) these dependent variables. Treatment was included as a fixed factor with random factors as described above. In addition, we assessed how potential and realized soil net Nmin were related to potential and realized soil net ammonification and nitrification, respectively. For this, we calculated site averages for each treatment separately. We then ran LMMs, with potential and realized soil net Nmin as the dependent variable, potential and realized soil net ammonification/nitrification as the independent ones. Site was included as a random factor.
Based on our previous work (Risch et al., 2019) and the existing literature (Schimel & Bennett, 2004; Liu et al., 2017), we developed a priori causal conceptual models of relationships among treatments, environmental drivers, and potential and realized soil net Nmin (Supplementary Fig. S2) to test with structural equation modelling (SEM) using a d-sep approach (Shipley, 2009; Lefcheck, 2016). The variables included in the model were long-term climatic conditions, specifically, site-level mean annual precipitation (MAP) and temperature of the wettest quarter (T.q.wet), plot-level soil texture (clay content) and soil microbial biomass. Mean annual precipitation and T.q.wet were obtained from WorldClim (Hijmans et al., 2005) (http://www.worldclim.org/) and together with the experimental treatments were predicted to directly affect soil properties and soil net Nmin (Supplementary Fig. S2). Soil clay content was, in turn, predicted to affect microbial biomass and soil net Nmin. Because we determined microbial biomass prior to incubating the samples in the laboratory or field, we assumed that the abundance of these microbes would be responsible for N process rates and not vice versa (Supplementary Fig. S2). We tested our conceptual model (Supplementary Fig. S2) using the piecewiseSEM package (version 2.0.2; Lefcheck, 2016) in R 3.4.0, in which a structured set of linear models are fitted individually. This approach allowed us to account for the nested experimental design, and overcome some of the limitations of standard structural equation models, such as small sample sizes (Shipley, 2009; Lefcheck, 2016). We used the lme function of the nlme package to model response variables, including site as a random factor. Good fit of the SEM was assumed when Fisher’s C values were non-significant (p > 0.05). For all significant interactions between covariates and experimental treatments detected in the SEMs, we calculated treatment effect sizes, i.e. the differences in potential or realized soil net Nmin between Control and treatments (Fence, NPK, NPK+Fence) and plotted these values against the climate or soil covariates. Finally, we fitted LMMs for the soil variables included in our SEMs, with treatment as the fixed factor, and with site and block as random factors, where block was nested within site.

en:
This dataset contains all data on which the following publication below is based.

Paper Citation:

Risch Anita C., Zimmermann, Stefan, Moser, Barbara, Schütz, Martin, Hagedorn, Frank, Firn, Jennifer, Fay, Philip A., Adler, Peter B., Biederman, Lori A., Blair, John M., Borer, Elizabeth T., Broadbent, Arthur A.D., Brown, Cynthia S., Cadotte, Marc W., Caldeira, Maria C., Davies, Kendi F., di Virgilio, Augustina, Eisenhauer, Nico, Eskelinen, Anu, Knops, Johannes M.H., MacDougall, Andrew S., McCulley, Rebecca L., Melbourne, Brett A., Moore, Joslin L., Power, Sally A., Prober, Suzanne M., Seabloom, Eric W., Siebert, Julia, Silveira, Maria L. , Speziale, Karina L., Stevens, Carly J., Tognetti, Pedro M., Virtanen, Risto, Yahdjian, Laura, Ochoa-Hueso, Raul (accepted). Global impacts of fertilization and herbivore removal on soil net nitrogen mineralization are modulated by local climate and soil properties. Global Change Biology

Please cite this paper together with the citation for the datafile.

We assessed how the removal of mammalian herbivores (Fence) and fertilization with growth-limiting nutrients (N, P, K, plus nine essential macro- and micronutrients; NPK) individually, and in combination (NPK+Fence), affected potential and realized soil net Nmin across 22 natural and semi-natural grasslands on five continents. Our sites spanned a comprehensive range of climatic and edaphic conditions found across the grassland biome. We focused on grasslands, because they cover 40-50% of the ice-free land surface and provide vital ecosystem functions and services. They are particularly important for forage production and C sequestration. Worldwide, grasslands store approximately 20-30% of the Earth’s terrestrial C, most of it in the soil (Schimel, 1995; White et al., 2000).

ammonification

display_name: ammonification

climate

display_name: climate

fertilization

display_name: fertilization

global-change

display_name: global-change

grassland

display_name: grassland

herbivore

display_name: herbivore

mineralization

display_name: mineralization

nitrification

display_name: nitrification

nitrogen

display_name: nitrogen

nutrient-network

display_name: nutrient-network

soil

display_name: soil

en: EnviDat is the WSL data portal providing unified and managed access to environmental monitoring and research data. The portal has the capability to host and publish data sets. Through the sharing of unique and high-value data sets worldwide, EnviDat fosters research and contributes to advancing environmental science.

en: Anthropogenic change and soil net N mineralization


latent-heat-flux-over-snow

maintainer: Sergi González-Herrero

title_for_slug: latent-heat-flux-over-snow

en: meteo-station central-asia swiss-alps meta meteo snow

en:
This file includes the datasets used to compare the methods. It includes:
- EC Postprocessed heat flux data from sonic anemometer and gas analyzer. Files named: [SITE]_(NO)WatVap_eddypro_OUT_[type].csv
- MOST Postprocessed data from SNOWPACK model. Files named [SITE]_[year]_[METHOD].smet
- Configuration files for SNOWPACK (.ini files) and Eddypro (.eddypro files)

[SITE] correspond to DISHMA/DISH or Alpine Valley, PLATEAU/PLAT for Antarctic Plateau, TAJ for Pamir mountains (no EC)
[type] correspond to fluxnet, full_output or qc_details
[METHOD] indicates the stability model used and/or the roughness length

en:
This file includes the Jupyter notebooks to reproduce the method and the figures of the paper. This consists in:
- 3 files for Alpine Valley
- 3 files for Antarctic Plateau
- 1 file for application at Pamir mountains

en:
This dataset contains three case studies where are compared the latent heat flux calculated using the Eddy Covariance (EC) method, the Monin-Obukhov Similarity Theory (MOST) and the modified Bowen-ratio method presented in the research paper "Using the sensible heat flux eddy covariance based exchange coefficient to calculate latent heat from moisture mean gradients overn snow". We include the datasets, the code and the ini files for reproduce the research.
The dataset contain two files in zip format:
 1. Sowftware-Heat_fluxes_on_snow: Jupyter notebooks to reproduce the method and the figures of the paper.
 2. data.zip: Datasets used to compare the methods

central-asia

display_name: central-asia

meta

display_name: meta

meteo

display_name: meteo

meteo-station

display_name: meteo-station

snow

display_name: snow

swiss-alps

display_name: swiss-alps

en: Latent Heat Flux over Snow


en: biogeochemical-cycling microbial-biomass drought c13-labeling plfa forest

en: Gao_Frank_C13 pulse labeling.xlsx

en:
Data of manuscript by Gao t al. : Drought resistance and resilience of rhizosphere communities in forest soils from the cellular to ecosystem scale – insights from 13C pulse labeling
Inludes data on 13C pulse-labeling experiment in young beech model ecosystems and a mature pine forest. Data of soil climate, total PLFA, 13C label strength in PLFA of pulse-labeling carried out under drought and after rewetting

en: Data of 13C-pulselabeling experiments in a young beech model ecosystem and a mature pine forest exposed to drought and rewetting. Data include microclimate during the experiment, total PLFA contents, d13C signatures in PLFA , microbial biomass, soil-respired CO2 measure during 30 days following 3-4 hour long pulse labeling with highly 13C-enriched CO2.

biogeochemical-cycling

display_name: biogeochemical-cycling

drought

display_name: drought

forest

display_name: forest

microbial-biomass

display_name: microbial-biomass

plfa

display_name: plfa

en: Gao_Drought resistance and resilience of rhizosphere communities_13C-PLFA


maintainer: Virginie Marques

en: fish-composition mediterraneaen edna marseille teleo marine

en: Data access

en: Please use cyberduck to download for the moment

en:
Description: Fish environmental DNA data set collected in 2022 in the Calanques National Park
The eDNA samples were collected in 2022 in two locations (Moyades, M−FPA and “Impérial du large”, I-LPA), during the winter (January- February), the summer (June to August)and fall (mid-September to November) seasons, with the sampling dates depending on the weather conditions. For the M−FPA, samples were collected between Moyades island and Riou island, while for the I-LPA, they were collected on the south side of the “Impérial du large” island. To account for the existing bathymetry, in the M−FPA the samples were taken at two sampling sites with depths of 20 and 40 m, while in the I-LPA they were taken at two sites with depths of 20 and 80 m.
At each site, in-situ filtration of seawater was performed using a double-head submersible pump (Subspace, Geneva, Switzerland; nominal flow of ca. 1 L/min) strapped to an underwater scooter with 2 VigiDNA 0.20 µm filtration capsules (SPYGEN, le Bourget du Lac, France), along with disposable sterile tubing. The samples were collected along two horizontal transects (up to 400 m in length) during each closed-circuit rebreather dive, enabling the filtration of a water volume of 15 L/filter per depth, as close as possible to the substrate. Two filter replicates were collected by two divers at each sampling site, except in two cases where bad weather conditions or logistical issues meant that only one replicate was sampled.
After the filtration, the remaining seawater was emptied from the capsule back on the boat and replaced by a 80 mL CL1 conservation buffer (SPYGEN, le Bourget du Lac, France). To prevent any contamination, a strict protocol was followed during the entire process, requiring disposable gloves and single-use filtration equipment. Finally, the samples were stored at room temperature. We followed a strict contamination control protocol in both field and laboratory stages. Each water sample processing included the use of disposable gloves and single-use filtration equipment to avoid any risk of contamination. Libraries were prepared with ligation using the MetaFast protocol (Fasteris).
Data content:
	* rawdata/: contains the raw reads for each individual sample. One archive contains the paired-end reads specified by the _R1 or _R2 suffix as well as individually tagged PCR replicates (if available) together with an archive containing all extraction and PCR blank samples of the library. Reads have been demultiplexed using cutadapt but not trimmed, individual demultiplexing tags and primers remain present in the sequences.
	* taxadata/: contains the table with all detected taxonomy for each sample after bioinformatic processing (see Polanco et al. 2020 for details; https://doi.org/10.1002/edn3.140) and associated field metadata.
	* metadata/: contains two metadata files, one related to the data collected in the field for each filter, and the second related to the sequencing process in the lab (including the tag sequence, library name, and marker information for each sample)

edna

display_name: edna

fish-composition

display_name: fish-composition

marine

display_name: marine

marseille

display_name: marseille

mediterraneaen

display_name: mediterraneaen

teleo

display_name: teleo

educ

en: Education, culture and sport

envidat

en: EnviDat: the Environmental Data Portal

en: Environmental DNA Marine France Calanques 2022


maintainer: Amelie Fees

en: avalanche glide-snow-avalanche snowpack-simulation avalanche-activity time-lapse-photography

en: Glide distances for opening glide-cracks

en: This folder contains all glide-cracks where glide-distances were extracted from time-lapse photographs. Glide-distances were calculated in x-direction (width) and y-direction (downslope, length) by georeferencing the images.

en: SNOWPACK simulations

en: SNOWPACK simulations (.pro and .smet) covering season 2008/09 to 2021/22 at 10 virtual locations on Dorfberg. The locations correspond to the most common glide-snow avalanche paths.

en: Glide-snow avalanche activity

en: Table that contains all glide-snow avalanche events that were detected in time-lapse photographs (season 2008/09 to 2021/22). The columns are explained in the README.txt

en: README

en: README.txt explaining the dataset and columns of tables in more detail.

en:
This dataset includes the processed data of the glide-snow avalanche activity and dynamics on Dorfberg (Davos, Switzerland) covering seasons 2008/09 to 2021/22. This dataset was described in the research article:

Fees, A., van Herwijnen A., Altenbach, M., Lombardo, M., Schweizer, J.: Glide-snow avalanche characteristics at different time-scales extracted from time-lapse photography, Annals of Glaciology, 91

We extracted the dynamics of opening glide-cracks and the glide-snow avalanche activity from time-lapse photographs. Glide-snow avalanches were separated into surface and interface events using the liquid water content which was simulated with SNOWPACK at 10 virtual stations on Dorfberg.

avalanche

display_name: avalanche

avalanche-activity

display_name: avalanche-activity

glide-snow-avalanche

display_name: glide-snow-avalanche

snowpack-simulation

display_name: snowpack-simulation

time-lapse-photography

display_name: time-lapse-photography

en: EnviDat is the WSL data portal providing unified and managed access to environmental monitoring and research data. The portal has the capability to host and publish data sets. Through the sharing of unique and high-value data sets worldwide, EnviDat fosters research and contributes to advancing environmental science.

en: Glide-snow avalanche activity on Dorfberg, Davos, Switzerland


en: complex-terrain orographic-precipitation precipitation-variability snow-precipitation cosmo-wrf

en: StationData

en: Snow depth maps over Dischma valley for 26 January 2016 and 9 March 2016 and snow depth differences between the two dates.

en:
The data presented here corresponds to the publication "Spatial variability in snow precipitation and accumulation in COSMO-WRF simulations and radar estimations over complex terrain" (Gerber et al., 2018a), which investigates the precipitation variability of snow precipitation in the central northern part of the Grisons (CH) and the publication "The importance of near-surface winter precipitation processes in complex alpine terrain" (Gerber et al., 2018b). The dataset contains:

* WRFsimulations: WRF simulation output for simulations with 4x (14x) terrain smoothing with an output timestep of 30 min/5 min and horizontal grid spacings of 1350 m, 450 m, 150 m and 50 m (currently: data available upon request).
* StationData: Meteorological station data of 18 meteorological stations in the central northern part of the Grisons with 30 minute resolution for the period 1 January 2016 till 1 May 2016.
* ADS80data: Photogrammetrically determined snow depth distribution data over the Dischma valley for the 26 January 2016 and 9 March 2016. Snow heights are corrected for buildings, vegetation (> 1m), outliers, and pixles, which are obivously snow-free on the pictures (Bühler et al., 2015). In addition the snow depth differences (snow depth on 9 March 2016 minus snow depth on 26 January 2016) are provided.

For more details about the simulation and observation data, see Gerber et al., 2018 and Gerber and Sharma (2018).

Publications:

Bühler, Y., Marty, M., Egli, L., Veitinger, J., Jonas, T., Thee, P., and Ginzler, C.: Snow depth mapping in high-alpine catchments using digital photogrammetry. Cryosphere, 9, 229–243, doi:10.5194/tc-9-229-2015, 2015.

Gerber, F., Besic, N., Sharma, V., Mott, R., Daniels, M., Gabella, M., Berne, A., Germann, U., and Lehning, M.: Spatial variability in snow precipitation and accumulation in COSMO-WRF simulations and radar estimations over complex terrain, The Cryosphere, 12, 3137–3160, doi:10.5194/tc-12-3137-2018, 2018.

Gerber, F., Mott, R. and Lehning, M.: The importance of near-surface winter precipitation processes in complex alpine terrain, Journal of Hydrometeorology, accepted, 2018.

Gerber, F., and Sharma, V.: Running COSMO-WRF on very-high resolution over complex terrain. Laboratory of Cryospheric Sciences CRYOS, École Polytechnique Fédérale de Lausanne EPFL, Lausanne, Switzerland. doi:10.16904/envidat.35, 2018.

complex-terrain

display_name: complex-terrain

cosmo-wrf

display_name: cosmo-wrf

orographic-precipitation

display_name: orographic-precipitation

precipitation-variability

display_name: precipitation-variability

snow-precipitation

display_name: snow-precipitation

en: DISCHMEX - High-resolution WRF simulations in complex alpine terrain and station measurements