maintainer: Lorenz Walthert

en: anisohydric water-use-strategy water-potential stomatal-stringency root-distribution

en: The data file contains the data shown in the Figures 2-7 in Walthert et al. (2024).

en:
This dataset represents the data shown in the Figures 2 - 7 of Walthert et al. (2024): Coordination between degree of isohydricity and depth of root water uptake in temperate tree species. Science of the Total Environment (https://doi.org/10.1016/j.scitotenv.2024.174346). A detailed methodical description of the data can be found in the Methods section of the paper.

Abstract
In an increasingly dry environment, it is crucial to understand how tree species use soil water and cope with drought. However, there is still a knowledge gap regarding the relationships between species-specific stomatal behaviour, spatial root distribution, and root water uptake (RWU) dynamics.
Our study aimed to investigate above- and below-ground aspects of water use during soil drying periods in four temperate tree species that differ in stomatal behaviour: two isohydric tracheid-bearing conifers, Scots pine and Norway spruce, and two more anisohydric deciduous species, the diffuse-porous European beech, and the ring-porous Downy oak. From 2015 to 2020, soil-tree-atmosphere-continuum parameters were measured for each species in monospecific forests where trees had no access to groundwater. The hourly time series included data on air temperature, vapour pressure deficit, soil water potential, soil hydraulic conductivity, and RWU to a depth of 2 m. Analysis of drought responses included data on stem radius, leaf water potential, estimated osmotically active compounds, and drought damage.
Our study reveals an inherent coordination between stomatal regulation, fine root distribution and water uptake. Compared to conifers, the more anisohydric water use of oak and beech was associated with less strict stomatal closure, greater investment in deep roots, four times higher maximum RWU, a shift of RWU to deeper soil layers as the topsoil dried, and a more pronounced soil drying below 1 m depth. Soil hydraulic conductivity started to limit RWU when values fell below 10-3 to 10-5 cm/d, depending on the soil. As drought progressed, oak and beech may also have benefited from their leaf osmoregulatory capacity, but at the cost of xylem embolism with around 50% loss of hydraulic conductivity when soil water potential dropped below -1.25 MPa. Consideration of species-specific water use is crucial for forest management and vegetation modelling to improve forest resilience to drought.

anisohydric

display_name: anisohydric

root-distribution

display_name: root-distribution

stomatal-stringency

display_name: stomatal-stringency

water-potential

display_name: water-potential

water-use-strategy

display_name: water-use-strategy

en: Water-use strategies of temperate tree species


maintainer: Ionut Iosifescu Enescu

en: jupyter-notebooks reproducibility research-data-management open-data hpc open-source open-science

state: active

type: dataset

en: Open Science Support @ WSL (Poster)

media_type: application/pdf

format: PDF

mimetype: application/pdf

en:
This poster was originally created for the swissuniversities Open Science Action Plan: Kick-Off Forum, and showed to the audience on 17.10.2019. It illustrates how the environmental data portal EnviDat provides the tools for fostering Open Science and Reproducibility of scientific research at WSL.

Supporting open science is a highly relevant user requirement for EnviDat and for implementing FAIR (Findability, Accessibility, Interoperability and Reusability) principles at dataset level.
EnviDat encourages WSL scientists to complement data publication with a complete description of research methods and the inclusion of the open source software, code or scripts used for processing the dataset or for obtaining the published results. By openly publishing open software (e.g. as Jupyter notebooks) alongside research data sets, researchers can contribute to mitigate reproducibility issues.

EnviDat also promotes and supports, where possible and practical, the publication of software as Jupyter notebooks. Jupyter notebooks provide a solution for improved documentation and interactive execution of open code in a wide range of programming languages (Python, R, Octave/Matlab, Java or Scala). These programming languages are widely used in environmental research at WSL and well supported by the Jupyter-compatible kernels. We have sucessfully interfaced EnviDat-hosted notebooks with the WSL High-Performance Computing (HPC) Linux Cluster through a JupyterHub/JuypterLab beta installation on the HPC cluster implemented in close collaboration with the WSL IT-Services.
For existing software that cannot be easily migrated to Jupyter Notebooks, the Open Science and Reproducibility is assisted by containerisation. We have proven that several Singularity containers can successfully run on WSL's HPC cluster.

Finally, the researchers can upload the data/results complemented by code (e.g. as Jupyter Notebooks, or Singularity containers) and any additional documentation in EnviDat. Consequently, they will receive a DOI for the entire dataset, which they can reference in their science paper in order to publish a more reproducible research.

_License_: This poster is released by WSL and the EnviDat team to the public domain under a Creative Commons 4.0 CC0 "No Rights Reserved" international license. You can reuse this poster in any way you want, for any purposes and without restrictions.

hpc

display_name: hpc

jupyter-notebooks

display_name: jupyter-notebooks

open-data

display_name: open-data

open-science

display_name: open-science

open-source

display_name: open-source

reproducibility

display_name: reproducibility

research-data-management

display_name: research-data-management

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: Open Science Support at the Swiss Federal Research Institute WSL. The EnviDat Concept


maintainer: EnviDat Support

en: flora endemism landscape-evolution geology madagascar

en: Escarpment evolution drives the diversification of the Madagascar flora

media_type: application/zip

en: This upload contains the data (species checklist, species range maps, time-calibrated phylogenies, topographic change, etc.) generated, analyzed, and presented in the paper .

format: ZIP

mimetype: application/zip

en: Data v1.0

en: Although much of the endemic biodiversity of Madagascar can be attributed to its isolation as an island in the Indian Ocean, the high rates of speciation throughout its geologic history suggest an influence of local-scale landscape dynamics. The topographic evolution of Madagascar is dominated by the formation of high-relief continental rift escarpment and we argue that the erosion and landward retreat of this topography creates habitat heterogeneity that has served as a speciation pump for the island. The highest plant richness is found along the escarpment and is characterized by steady diversification rates over the last 45 Ma. Modeled landscape evolution by escarpment retreat demonstrates opportunities for allopatric speciation by transient habitat fragmentation through multiple mechanisms, including catchment expansion, isolation of highland remnants and formation of topographic and river barriers The segregation of floral phylogenetic turnover parallel to the escarpment is consistent with these mechanisms and indicates the importance of erosion-driven landscape dynamics on speciation.

endemism

display_name: endemism

flora

display_name: flora

geology

display_name: geology

landscape-evolution

display_name: landscape-evolution

madagascar

display_name: madagascar


en: plants phylogenetic-diversity taxonomic-diversity zonation migclim conservation land-use-change european-alps functional-diversity species-distribution-models beta-diversity global-change

en: Updated SDM outputs

en: Refined scenarios of plants distribution in the European Alps

format: GeoTIFF

en: Data Access

en:
This repository contains extensive data for the European Alps:
  - Observations of ~3,500 plant species
  - Climate (1-km), soil (100-m) and land cover predictors (1km); current and future scenarios (28 CMIP6-GCMs, 2 land cover change and 3 dispersal scenarios i.e., unlimited, no and realistic vegetation dispersal)
  - Flora migration rates (categorical) and ecological preferences (continuous indicator values)
  - Regional maps of barriers to migration and water bodies at 100-m resolution
  - Sampling effort, distance to roads and cities predictors at 100-m resolution
  - Present and future abundances over the study region at 1-km resolution (~2,000 species)
  - Present and future multifaceted and uniqueness of the European Alps' Flora at 1-km resolution
  - Present and future conservation recommendations at 1-km resolution (26 current and future strategies)
  - Phylogenetic data and functional traits of ~2,000 plants (raw data and classification trees)
  - All scripts, data and plots used for the analyses, including a singularity container (mini-linux) to run them

beta-diversity

display_name: beta-diversity

conservation

display_name: conservation

european-alps

display_name: european-alps

functional-diversity

display_name: functional-diversity

global-change

display_name: global-change

land-use-change

display_name: land-use-change

migclim

display_name: migclim

phylogenetic-diversity

display_name: phylogenetic-diversity

plants

display_name: plants

species-distribution-models

display_name: species-distribution-models

taxonomic-diversity

display_name: taxonomic-diversity

zonation

display_name: zonation

en: Present and future multifaceted plant diversity, uniqueness and conservation in the European Alps


maintainer: Frank Techel

en: verification avalanche-forecasting avalanche-bulletin avalanche-danger-level avalanche-forecast

en: D_QC for forecasting seasons 2020/2021 - 2022/2023.

format: XLS

en: Data for the 2023/2024 forecasting season. It was added on 26 Aug 2024 by F. Techel.

en: D_QC for forecasting seasons 2001/2002 until 2019/2020.

en:
The data set contains the re-analyzed (or quality-checked) regional avalanche danger levels (D_QC) for Switzerland.

D_QC relates to dry-snow avalanche conditions only. Measuring the avalanche danger level D is not possible; forecast, nowcast, and hindcast assessments of D are judgments by humans interpreting data. However, combining several pieces of information indicating the same D, it can be expected that it is more likely that D_QC represents the avalanche conditions well.

For the **forecasting seasons 2001/2002 until 2019/2020**, the approach to obtain D_QC is described in detail in Appendix A of [Pérez-Guillén et. al. (2022)](https://nhess.copernicus.org/articles/22/2031/2022/nhess-22-2031-2022.html).

For the **forecasting seasons 2020/2021 and later**, D_QC is derived using the following approach:
1. *Combination of forecast (D_forecast) and nowcast (D_nowcast)*: If there was only one assessment available by an observer after a day in the field for a region, and if D_forecast = D_nowcast --> D_QC = D_forecast.
2. *Combination of several nowcast assessments (D_nowcast)*: If two (or more) observers agreed (or majority opinion) in their (independent) assessments of D_nowcast after a day in the field in the same warning region. --> D_QC = D_nowcast.
3. *Hindcast analysis (D_hindcast)*: In Switzerland, avalanche forecasters re-evaluate all situations when D = 4 (high) or D = 5 (very high) were either forecast, should have been forecast, or when forecasters discussed given one of these two levels but had not given them. Generally, two forecasters assess each situation. In these cases, D_QC = D_hindcast. The hindcast analysis, only available since the forecasting season 2020/2021, replaces what was step (2) in Appendix A of [Pérez-Guillén et. al. (2022)](https://nhess.copernicus.org/articles/22/2031/2022/nhess-22-2031-2022.html).

All other cases - ties in case of (1) or (2), no new information from the warning region in question, or if no D_hindcast was available - are not considered quality-checked, and are, thus, not contained in the data set.

In addition to D_QC, the file contains information on the elevation and aspect, where D_QC likely prevails.
- The indicated elevation is the mean of the respective elevations in (1), (2), or (3). At danger level 1 (low), when no elevation is indicated in the Swiss forecast, a value of 1500 m is set.
- For the four cardinal aspects N, E, S, and W, a value of 1 means that there was agreement that D was reached in this aspect and a value of 0 means that there was agreement that D was not reached in this aspect. Intermediate values correspondingly mark disagreements in the assessments.

avalanche-bulletin

display_name: avalanche-bulletin

avalanche-danger-level

display_name: avalanche-danger-level

avalanche-forecast

display_name: avalanche-forecast

avalanche-forecasting

display_name: avalanche-forecasting

verification

display_name: verification

en: Re-analyzed regional avalanche danger levels in Switzerland


maintainer: Yohann Chauvier

en: climate ecological-indicator-values taxonomic-diversity functional-diversity grain-size soil phylogenetic-diversity

en: Data access

en:
This dataset comprises a large array of ecological data for the European Alps:

  (1) Current soil and climate predictors at various resolutions.
  (2) GBIF observations of the European Alps Flora (~4,000 species).
  (3) Species habitat suitability maps (1,109 species; based on species observations filtered at 40x40-km)
  at various resolutions used in the study to generate (4); except 'expert'...
  (4) Expert, Taxonomic, phylogenetic and functional diversity of the study region at various resolutions
  (from 100-m to 40-km --> 100-m aggregated & mean to km + non-aggregated/predicted) for CLIM,
  SOIL and CLIM-SOIL models.
  (5) Ecological and altitudinal preferences of the European Alps Flora.
  (6) Data outputs of the related published article.
  (7) All scripts used for analyses.
  (8) Additional files used for analyses.
  (9) Improved set of species habitat suitability maps (~2,600 species; based on species observations
  filtered at 1x1-km) and related taxonomic diversity at 100-m resolution (aggregated to km +
  non-aggregated/predicted) for CLIM, SOIL and CLIM-SOIL models ---> not incorporated in the study.

climate

display_name: climate

ecological-indicator-values

display_name: ecological-indicator-values

grain-size

display_name: grain-size

soil

display_name: soil

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: Resolution in species distribution models shapes spatial patterns of plant multifaceted diversity


en: slow-snow-compression-experiments microstructure x-ray-tomography snow-mechanics ice

en: README

media_type: text/plain

en: README file gives an overview of the organization of the data

format: TXT

en: slow snow compression experiments

en: Compression experiments, X-ray images and with supplemented README file

en:
We conducted consecutive loading-relaxation experiments at low strain rates to study the viscoplastic behavior of the intact ice matrix in snow. The experiments were conducted using a micro-compression stage within the X-ray tomography scanner in the SLF cold laboratory.

Next, to evaluate the experiments, a novel, implicit solution of a transient scalar model was developed to estimate the stress exponent and time scales in the effective creep relation (Glen's law). The result reveals that, for the first time, a transition in the exponent in Glen's law depends on geometrical grain size. A cross-over of stress exponent $n=1.9$ for fine grains to $n=4.4$ for coarse grains is interpreted as a transition from grain boundary sliding to dislocation creep.

The dataset includes compression force data from 11 experiments and corresponding 3D image data from tomography scans.

ice

display_name: ice

microstructure

display_name: microstructure

slow-snow-compression-experiments

display_name: slow-snow-compression-experiments

snow-mechanics

display_name: snow-mechanics

x-ray-tomography

display_name: x-ray-tomography

en: A grain-size driven transition in the deformation mechanism in slow snow compression


maintainer: Tessa Hegetschweiler

en: recreational-activities adolescents teenagers forest childhood

en: Dataset comments

en: The codebook to the dataset

en: Questionnaire school survey

en: The questionnaire used in the survey at 8 schools aimed at teenagers in German.

en: Dataset survey at schools

en: The dataset of the questionnaire survey at schools in excel format.

en: Survey at schools 2017

en: The dataset of the questionnaire survey at schools in SPSS-format.

format: SERVICE

en: The data results from a questionnaire survey conducted at 8 schools in the cantons Zurich, Aargau and St. Gallen. Respondents aged 13-22 years. The aim of the survey was to gain insight into teenagers' relationship to the forest, reasons for visiting or not visiting the forest and activities in the forest.

adolescents

display_name: adolescents

childhood

display_name: childhood

forest

display_name: forest

recreational-activities

display_name: recreational-activities

teenagers

display_name: teenagers

en: Factors influencing teenagers' forest visit frequency


en: reservoir-inflow forecast-models renewable-energy solar-irradiance meteorological-data hydropower electricity-grid

en: ERA5 Land, Seasonal forecast and short-term forecast meteorological data to train inflow and residual demand forecast models.

en: Description of Swissgrid high-voltage (>150kV) grid, including lines, transformers and nodes (snapshot of the grid in 2019) .

en: Plants and reservoirs description, with associated hourly inflows (2009 - 2019).

en: Data structure and description.

en: Solar irradiance maps projected onto tilted surfaces: hourly time series for 35° and 65° tilts, azimuth 180°. (same method as [Frischholz, Y. (2025)](https://www.doi.org/10.16904/envidat.632))

en:
This dataset contains several useful components for **Swiss Electricity system modeling**:
1. **High-voltage Swiss grid**: 2019 snapshot of the high-voltage (>150kV) grid composed of :
- Nodes: names, voltage, position.
- Lines: ends nodes, resistance, power capacity.
- Transformers: ends nodes, power capacity, resistance, tap ratio.
2. **Hydropower topology** : Representative description of Swiss reservoirs and plants (2019) composed of:
- Plants: Lower reservoir, Upper reservoir, pump/turbine, debit, power capacity.
- Reservoirs: Volume, altitude, position, canton.
3. **Inflows** into all the reservoirs: hourly time series post-processed from PREVAH model outputs from 2009 to 2019.
4. **Wind production per node**: COSMO-1 data processed and scaled to match SFOE annual production.
5. **Solar irradiance maps projected onto tilted surfaces**: hourly time series for 35° and 65° tilts, azimuth 180°. (same method as [Frischholz, Y. (2025)](https://www.doi.org/10.16904/envidat.632))
6. **Processed ERA5 (historical), ECMWF SEAS5 (seasonal forecast) and ECMWF TIGGE (short-term forecast)**:
- ERA5 Land: For inflow forecast model: historical runoff, snow depth, temperature and total precipitation per catchment (hourly, 2009-2019). For residual demand forecast model: historical temperature, u-v wind, ssrd per country (CH, AT, DE, FR, IT, hourly 2015-2019)
- ECMWF SEAS5: For inflow forecast model: same variables as ERA5 (yearly forecast starting from every 1st day of every month in 2019). For residual demand forecast model: same variables as ERA5 (yearly forecast starting from every 1st day of every month in 2019).
- ECMWF TIGGE: For inflow forecast model: same variables as ERA5 (two weeks forecast starting from every 1st day of every week in 2019). For residual demand forecast model: same variables as ERA5 (two weeks forecast starting from every 1st day of every week in 2019).
\
More details can be found on *README.txt*.

electricity-grid

display_name: electricity-grid

forecast-models

display_name: forecast-models

hydropower

display_name: hydropower

meteorological-data

display_name: meteorological-data

renewable-energy

display_name: renewable-energy

reservoir-inflow

display_name: reservoir-inflow

solar-irradiance

display_name: solar-irradiance

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: Swiss electricity system modeling -- HV grid - hydropower topology and inflows - renewable productions - past and forecast meteorological data


en: metabarcoding atlantic-region bayofbiscay chondrichthyes actinopterygii fish-composition edna teleo

en: Data access

en:
Environmental DNA complements scientific trawling in surveys of marine fish biodiversity (Dataset 2019)
In October 2019 we chose 15 sites from the 2019 EVHOE survey for eDNA sampling. The French international EVHOE bottom trawl survey is carried out annually during autumn in the BoB to monitor demersal fish resources. At each site, we sampled seawater using Niskin bottles deployed with a circular rosette. There were nine bottles on the rosette, each of them able to hold ∼5 l of water. At each site, we first cleaned the circular rosette and bottles with freshwater, then lowered the rosette (with bottles open) to 5 m above the sea bottom, and finally closed the bottles remotely from the boat. The 45 l of sampled water was transferred to four disposable and sterilized plastic bags of 11.25 l each to perform the filtration on-board in a laboratory dedicated to the processing of eDNA samples. To speed up the filtration process, we used two identical filtration devices, each composed of an Athena® peristaltic pump (Proactive Environmental Products LLC, Bradenton, Florida, USA; nominal flow of 1.0 l min–1 ), a VigiDNA 0.20 μm filtration capsule (SPYGEN, le Bourget du Lac, France), and disposable sterile tubing. Each filtration device filtered the water contained in two plastic bags (22.5 l), which represent two replicates per sampling site. We followed a rigorous protocol to avoid contamination during fieldwork, using disposable gloves and single-use filtration equipment and plastic bags to process each water sample. At the end of each filtration, we emptied the water inside the capsule that we replaced by 80 ml of CL1 conservation buffer and stored the samples at room temperature following the specifications of the manufacturer (SPYGEN, Le Bourget du Lac, France). We processed the eDNA capsules at SPYGEN, following the protocol proposed by Polanco-Fernández et al., (2020). We performed library preparation and sequencing at Fasteris (Geneva, Switzerland). Specifically, we prepared four libraries using the MetaFast protocol (a ligation-based method) and sequenced them separately. We carried out paired-end sequencing using a MiSeq sequencer (2 × 125 bp, Illumina, San Diego, CA, USA) on two MiSeq Flow Cell Kits (v3; Illumina), following the manufacturer’s instructions. We analysed the sequence reads using the OBITools package (http://metabarcoding.org/obitools; Boyer et al., 2016), following the protocol described by Valentini et al. (2016).
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)

actinopterygii

display_name: actinopterygii

atlantic-region

display_name: atlantic-region

bayofbiscay

display_name: bayofbiscay

chondrichthyes

display_name: chondrichthyes

edna

display_name: edna

fish-composition

display_name: fish-composition

metabarcoding

display_name: metabarcoding

teleo

display_name: teleo

en: Environmental DNA Marine France Evhoe 2019


en: potential-evapotranspiration chelsa extreme-events drought megadrought precipitation multi-year-drought

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

en: Standardized Precipitation Index (SPI)

en: Global monthly layers of the Standardized Precipitation Index (SPI) a 30 arcsec (~1km) spatial resolution

en: Kernel Normalized Difference Vegetation Index Anomaly (QKNDVI)

en: Global annual layers of the the kernel normalized difference vegetation index anomaly (qkndvi) at a 1/12° (~10km) spatial resolution.

en: Statistics of the multiyear meteorological droughts, containing the ID, duration, area, and empirical ranking of the droughts.

en: Multiyear meteorological droughts (MYMD10) statistics - Description

en: Description of column names, and units of the fields contained in the dataset "Multiyear meteorological droughts (MYMD10) statistics".

en: Standardised Precipitation Evapotranspiration Index (SPEI)

en: Global monthly layers of the Standardized Precipitation Evapotranspiration Index (SPEI) a 30 arcsec (~1km) spatial resolution

en: Multiyear meteorological droughts (MYMD) statistics - Description

en: Description of column names, and units of the fields contained in the dataset "Multiyear meteorological droughts (MYMD) statistics".

en: Global annual layers of the multiyear meteorological droughts (MYMD) at a 1/24° (~5km) spatial resolution

en:
Multiyear meteorological droughts (MYMD10) statistics
Statistics of the multiyear meteorological droughts, containing the ID, duration, area, and empirical ranking of the droughts, and the anomalies in kNDVI

en: Global annual layers of the multiyear meteorological droughts (MYMD) at a 1/12° (~10km) spatial resolution

en:
The dataset consists of the standardized precipitation (SPI) and the standardized precipitation evapotranspiration index (SPEI) index with a 30 arcsec (~1km) horizontal resolution.
Data for precipitation rates (pr) and potential evapotranspiration (pet) are taken from CHELSA V2.1 (https://doi.org/10.16904/envidat.228.v2.1). Both data sets are monthly time series from 1980 to 2018 at 30 arcsec. and have the unit of kg m-2 month-1. SPEI is a more reliable measure of drought than SPI as it additionally considers the effect of potential evapotranspiration. Potential evapotranspiration (pet) is the amount of water per area per time that can evaporate at the soil surface or be transpired by plants in absence of water supply limitations. SPEI effectively estimates for a given location how the climatic water balance, i.e., the difference between precipitation rate (pr) and potential evapotranspiration (pet), relates to the long-term mean. Here, pet was calculated with the Penman-Montheith approach, assuming surface conductance of a reference crop of 12 cm height following the definition of the Food and Agriculture Organization of the United Nations (FAO), originating from CHELSA-BIOCLIM+ database (https://www.doi.org/10.16904/envidat.332). To obtain global time series of SPEI, in each pixel the frequency distribution of water balance estimates (pr-pet) is approximated with a log-logistic probability distribution function. We calculate monthly SPEI using a 12-month memory and approximate the parameters of the log-logistic probability distribution based on the time series from 1980-2018. Such a 12-month time window is suitable to capture long-term drought events that are long enough to impose substantial impacts on agriculture, hydrology, and ecosystems while ones at shorter time scales would be more appropriate to detect short-term drought. For each month, SPEI is calculated considering the respective water-balance value and the values of the eleven preceding months. Here we use SPEI-12 in December to represent the overall water-balance condition of the respective year. The resulting SPEI data has a horizontal resolution of 130 arcsec (~1km). The calculation of SPI and SPEI is done in R with the package SPEI (https://www.doi.org/10.32614/CRAN.package.SPEI).

chelsa

display_name: chelsa

drought

display_name: drought

extreme-events

display_name: extreme-events

megadrought

display_name: megadrought

multi-year-drought

display_name: multi-year-drought

potential-evapotranspiration

display_name: potential-evapotranspiration

precipitation

display_name: precipitation

en: High resolution global standardized drought indices


en: belowground-biomass afforestation picea-abies isotopes subalpine

en: This data set provides soil organic carbon, total nitrogen, and stable carbon isotope (13C) values of mineral soil (0-45cm), organic horizons (Oi, Oe, Oa), and root biomass of an afforestation sequence (0-130years) on a subalpine pasture in Jaun, Switzerland.

afforestation

display_name: afforestation

belowground-biomass

display_name: belowground-biomass

isotopes

display_name: isotopes

picea-abies

display_name: picea-abies

subalpine

display_name: subalpine

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: Soil organic carbon stock of an afforestation sequence on a subalpine pasture


maintainer: Anita Risch

en: exclusion grassland invertebrates subalpine ecosystem-functions grazing ecosystem-coupling swiss-national-park ecosystem-multifunctionality vertebrates

en: Datafile

en:
ID: Plot ID composited of Fence & Treatment number (90 plots total)

Grassland: Name of the six subalpine grasslands where the exclosure setups were erected. In large grasslands (GRIM, MING, STAB), we established four hierarchical exclosure setups (two in short- and two in tall-grass vegetation), whereas in the small grasslands (BOTS, DADA, MARG) only one setup was erected per vegetation type. BOTS = Val dal Botsch, GRIM = Grimmels, MING = Val Mingér, STAB = Alp Stabelchod, DADA = Stabelchod da daint, MARG = Margunet

Fence: Number of exclosure setup (1 - 18). Note that uneven numbers (1,3,5,7,9,11,13,15,17) represent setups established on short-grass vegetation, even numbers (2,4,6,8,10,12,14,16,18) setups established in tall-grass vegetation
Vegetation	Vegetation type, 1 = short-grass vegetation, 2 = tall-grass vegetation; (9 replicate fences on each vegetation type)
Treatment	Progressive animal exclusion, numbers indicate which animals had access to the plot: 1 = Large/medium/small mammals, and invertebrates have access ("L/M/S/I"), 2 = Medium/small mammals, and invertebrates have access (“M/S/I”), 3 = Small mammals and invertebrates have access (“S/I”), 4 = Invertebrates have access (“I”), 5 = No animals have access (“None”)

Bulkden:	Fine fraction soil bulk density (g cm-3)

Soil.moist	: Soil moisture (%)

Soil.org.C: Rhizosphere soil C content (%)

pH: Soil pH

Nema.PC1: First principal component (PC1) of principal component analysis (PCA) of the soil nematode community composition

Nema.PC2: Second principal component (PC2) of principal component analysis (PCA) of the soil nematode community composition

Micro.PC1: 	First principal component (PC1) of principal component analysis (PCA) of the soil microbial community composition

Micro.PC2: Second principal component (PC2) of principal component analysis (PCA) of the soil microbial community composition

Abv.Inv.PC1: First principal component (PC1) of principal component analysis (PCA) of the aboveground-dwelling invertebrate community composition

Abv.Inv.PC2: Second principal component (PC2) of principal component analysis (PCA) of the aboveground-dwelling invertebrate community composition

Arthr.PC1: First principal component (PC1) of principal component analysis (PCA) of the soil arthropod community composition

Arthr.PC2: Second principal component (PC2) of principal component analysis (PCA) of the soil arthropod community composition

Plant.PC1: First principal component (PC1) of principal component analysis (PCA) of the plant community composition

Plant.PC2: Second principal component (PC2) of principal component analysis (PCA) of the plant community composition

Root.biomass: Root biomass (g m-2)

Micro.biomass	: Microbial biomass carbon (mg kg-1)

Plant.richness: Plant species richness

Plant.N: Plant tissue nitrogen content (%)

Soil.N.min: Soil net nitrogen mineralisation (kg ha-1 season)

Soil.resp: Soil carbon dioxide emissions (soil respiration; g m-2 h-1)

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

Paper Citation:
 > Risch AC, Ochoa-Hueso R, van der Putten WH, Bump JK, Busse MD, Frey B, Gwiazdowicz DJ, Page-Dumroese DS, Vandegehuchte ML, Zimmermann S, Schütz M. Size-dependent loss of aboveground animals differentially affects grassland ecosystem coupling and functions. 2018. Nature Communications 9: 3684. [doi: 10.1038/s41467-018-06105-4](https://doi.org/10.1038/s41467-018-06105-4).

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

#Methods
Study sites
The experimental exclosure setups were installed within the SNP (IUCN category Ia preserve; Dudley 2008), in south-eastern Switzerland. The park covers 172 km2 of forests and subalpine and alpine grasslands along with scattered rock outcrops and scree slopes. The entire area has been protected from human impact (no hunting, fishing, camping or off-trail hiking) since 1914. Large, fairly homogenous patches of short- and tall-grass vegetation, which originate from different historical management and grazing regimes, cover the park’s subalpine grasslands entirely. Short-grass vegetation developed in areas where cattle used to rest (nutrient input) prior to the park’s foundation (14th century to 1914) (Schütz and others 2003, 2006) and is dominated by lawn grass species such as Festuca rubra L., Briza media L. and Agrostis capillaris L. (Schütz and others 2003, 2006). Today, this vegetation type is intensively grazed by diverse vertebrate and invertebrate communities that inhabit the park and consume up to 60% of the available biomass (Risch and others 2013). Tall-grass vegetation developed where cattle formerly grazed, but did not rest, and is dominated by rather nutrient-poor tussocks of Carex sempervirens Vill. and Nardus stricta L. (Schütz and others 2003, 2006). This vegetation type receives considerably less grazing, with only roughly 20% of the biomass consumed (Risch and others 2013). Consequently, the two vegetation types together represent a long-term trajectory of changes in grazing regimes. Underlying bedrock of all grasslands is dolomite, which renders these grasslands rather poor in nutrients regardless of former and current land-use regimes.
Experimental design
To progressively exclude aboveground vertebrate and invertebrate animals, we established 18 size-selective exclosure setups (nine in short-grass, nine in tall-grass vegetation) distributed over six subalpine grasslands across the SNP (Risch and others 2013, 2015). Elevation differences of exclosure locations did not exceed 350 m (between 1975 and 2300 m a.s.l.). The exclosures were established immediately after snowmelt in spring 2009 and were left in place for five consecutive growing seasons (until end of 2013). They were, however, temporarily dismantled every fall (late October after first snowfall) to protect them from avalanches. They were re-established in the same location every spring immediately after snowmelt. Each size-selective exclosure setup consisted of five plots (2 x 3 m) that progressively excluded aboveground vertebrates and invertebrates from large to small. The plots are labelled according to the guilds that had access to them “L/M/S/I”, “M/S/I”, “S/I”, “I”, “None”; L = large mammals, M = medium mammals, S = small mammals, I = invertebrates, None = no animals had access. As we only had permission to have the experimental setup in place for five consecutive growing seasons, the experiment had to be completely dismantled in the late fall of 2013 and all material removed from the SNP.
Our exclosure design was aimed at excluding mammalian herbivores, but naturally also excluded the few medium and small mammalian predators, as well as the entire aboveground invertebrate food web. A total of 26 large to small mammal species can be found in the SNP, but large apex predators are missing (wolf, bear, lynx) . Reptiles, amphibians and birds are scarce to absent in the subalpine grasslands under study. Only two reptile species occur in the park and they are confined to rocky areas that warm up enough for them to survive. One frog species spawns in an isolated pond far from our grasslands. Only three bird species occasionally feed on the subalpine grasslands. Using game cameras (Moultrie 6MP Game Spy I-60 Infrared Digital Game Camera, Moultrie Feeders, Alabaster, AL, USA), we did observe that the medium- and small-sized mammals (marmot/hares and mice) were not afraid to enter the fences and feed on their designated plots. We never spotted reptiles, amphibians or birds on camera. We distinguished between 59 higher aboveground-dwelling invertebrate taxa that our size-selective exclosures excluded (see also methods for aboveground-dwelling invertebrates below).
The “L/M/S/I” plot (not fenced) was located at least 5 m from the 2.1 m tall and 7 x 9 m large main electrical fence that enclosed the other four plots. The bottom wire of this fence was mounted at 0.5 m height and was not electrified to enable safe access for medium and small mammals, while fencing out the large ones. Within each main fence, we randomly established four 2 x 3 m plots separated by 1-m wide walkways from one another and from the main fence line: 1) the “M/S/I” plots were unfenced, allowing access to all but the large mammals; 2) the “S/I” plots (10 x 10 cm electrical mesh fence) excluded all medium-sized mammals. Note that the bottom 10 cm of this fence remained non-electrified to enable safe access for small mammals; 3) the “I” plots (2 x 2 cm metal mesh fence) excluded all mammals. We double-folded the mesh at the bottom 50 cm to reduce the mesh size to smaller than 1 x 1 cm openings; and 4) the “None” plots were surrounded by a 1 m tall mosquito net (1.5 x 2 mm) to exclude all animals. The top of the plot was covered with a mosquito-meshed wooden frame mounted to the corner posts (roof). We treated these plots a few times with biocompatible insecticide (Clean kill original, Eco Belle GmbH, Waldshut-Tiengen, Germany) to remove insects that might have entered during data collection or that hatched from the soil, but amounts were negligible and did not impact soil moisture conditions within these plots.
To assess whether the design of the “None” exclosure (mesh and roof) affected the response variables within the plots and, therefore, influenced the results, we established an additional six “micro-climate control” exclosures (one in each of the six grasslands) (Risch and others 2013, 2015). These exclosures were built as the “None” exclosures but were open at the bottom (20 cm) of the 3-m side of the fence facing away from the prevailing wind direction to allow invertebrates to enter. A 20-cm high and 3-m long strip of metal mesh was used to block access to small mammals. Thus, this construction allowed a comparable micro-climate to the “None” plots, but also a comparable feeding pressure by invertebrates to the “I” plots. We compared various properties within these exclosures against one another to assess if our construction altered the conditions in the “None” plots. We showed that differences in plant (e.g., vegetation height, aboveground biomass) and soil properties (e.g., soil temperature, moisture) found between the “I” and the “None” treatments were not due to the construction of the “None” exclosure, but a function of animal exclusions, although the amount of UV light reaching the plant canopy was significantly reduced (Risch and others 2013).
Aboveground invertebrate sampling
Aboveground invertebrates were sampled with two different methods to capture both ground- and plant-dwelling organisms: 1) we randomly placed two pitfall traps (67 mm in diameter, covered with a roof) filled with 20% propylene glycol in one 1 x 1 m subplot of the 2 x 3 m treatment plots in spring 2013 (May) and emptied them every two weeks until late September 2013 (Vandegehuchte and others 2017b, 2018). A pitfall trap consisted of a plastic cylinder (13 cm depth, 6.75 cm diameter). Within each cylinder we placed a 100 ml plastic vial with outer diameter 6.70 cm and on top of the cylinder we placed a plastic funnel to guide the invertebrates into the vials. Each trap was cover with a cone-shaped and transparent plastic roof to protect the trap from rain (Vandegehuchte and others 2017b, 2018). Note that in the “None” plots only one trap was placed as control to check for effectiveness of the exclosure. 2) We vacuumed all invertebrates from a 60 x 60 cm area on another 1 x 1 m subplot with a suction sampler (Vortis, Burkhard manufacturing CO, Ltd., Rickmansworth, Hertfordshire, UK) every month from June to September 2013 (Vandegehuchte and others 2017b, 2018). For this purpose, we quickly placed a square plastic frame (60 x 60 x 40 cm) with a closable mosquito mesh sleeve attached to the top edge into the plot from the outside. The suction sample was then inserted into through the sleeve and operated for 45 s to collect the invertebrates (Vandegehuchte and others 2017b, 2018).
We sorted the ≈100 000 individuals collected with both methods by hand and identified each individual morphologically to the lowest taxonomic level feasible (59 taxa, including orders, suborders, subfamilies, families; phylum for Mollusca). These taxa belonged to the following feeding types: 19 herbivores, 16 detritivores, 9 predators, 8 mixed feeders, 5 omnivores and 2 non-classified feeders (or not feeding as adults) (Vandegehuchte and others 2017b). We summed the numbers from the two pitfall traps and the suction sampling over the course of the 2013 season to represent the aboveground invertebrate abundance and community composition of a plot. Note: we did not specifically attempt to catch flying invertebrates with e.g., sticky traps, thus a few flying insects may have been missed with our vacuum sampling approach.
Sampling of plant properties
The vascular plant species composition was assessed at peak biomass every summer (July) by estimating the frequency of occurrence of each species with the pin count method in each plot (Frank and McNaughton 1990). A total of 172 taxa occurred within our 90 plots and we calculated plant species richness for each plot separately. We used the 2013 data in this study. Plant quality was assessed every year in July and September; here we use plant quality at the end of the experiment (September 2013). Two 10 x 100 cm wide strips of vegetation per plot were clipped, combined, dried at 65°C, and ground (Pulverisette 16, Fritsch, Idar-Oberstein, Germany) to pass through a 0.5 mm sieve. Twenty randomly selected samples across all treatments were analysed for N (Leco TruSpec Analyser, Leco, St. Joseph, Michigan, USA) (Vandegehuchte and others 2015). Nitrogen concentrations of the other samples were then estimated from models established for the experiment and the entire SNP relating Fourier transform-near infrared reflectance (FT-NIR) spectra to the measured values of N using a multi-purpose FT-NIR spectrometer (Bruker Optics, Fällanden, Switzerland) (Vandegehuchte and others 2015). Root biomass was sampled every fall by collecting five 2.2 cm diameter x 10 cm deep soil samples (Giddings Machine Company, Windsor, CO, USA) per plot (450 samples year-1). The samples were dried at 30 °C and roots were sorted from the sample by hand. We sorted each sample for 1 h which allowed to retrieve over 90% of all roots present in the samples (Risch and others 2013). The roots were then dried at 65 °C for 48 and weighed to the nearest mg. We averaged the values per plot and used the 2013 data only in this study.
Sampling of edaphic communities
In 2009, 2010, and 2011 we collected three composited soil samples (5 cm diameter x 10 cm depth; AMS Samplers, American Falls, ID, USA) and assessed bacterial community structure using T-RFLP profiling (Liu and others 1997; Blackwood and others 2003; Hodel and others 2014). We detected a total of 89 operational taxonomic units (OTUs). These values are in accordance with other studies reporting OTU richness (Wirthner and others 2011; Zumsteg and others 2012; Meola and others 2014) using T-RFLP profiling, a method that detects the most abundant, and thus likely, the most relevant, taxa. We averaged the data over the three years of collections for our calculations. Microbial biomass carbon (MBC) was determined with the substrate-induced method (Anderson and Domsch 1978) every fall (September) between 2009 and 2013 by collecting three mineral soil samples (5 cm diameter × 10 cm mineral soil core, AMS Samplers, American Falls, ID, USA). The three samples were combined (90 samples for each sampling year), immediately put on ice, taken to the laboratory, passed through a 2-mm sieve and stored at 4°C. Again, we only used the 2013 data in this study.
Soil samples (5 cm diameter x 10 cm depth) to extract soil arthropods were collected in June, July, and August 2011 with a soil corer lined with a plastic sleeve to ensure an undisturbed sample (total of 270 samples). The plastic line core was immediately sealed on both ends using cling film and put into a cooler. All plots were sampled within three days and the extraction of arthropods started the evening of the sampling day using a high-gradient Tullgren funnel apparatus (Crossley and Blair 1991; Vandegehuchte and others 2015). Samples were kept in the extractor for four days and the soil arthropods were collected in 95% ethanol. All individuals were counted and each individual was identified morphologically to the lowest level feasible [76 taxa, including orders, suborders, subfamilies, families (Protura, Thysanoptera, Aphidina, Psylina, Coleoptera, Brachycera, Nematocera, Auchenorryncha, Heteroptera, Formicidae); sub-phylum for Myriapoda, for Acari and Collembola also including morpho-species). Note that we also included larval stages (nine of the 76 taxa) (Vandegehuchte and others 2015). All data were summed over the season. A detailed species list for mites and collembolans is published (Vandegehuchte and others 2017a) [https://doi.org/10.1371/journal.pone.0118679.s001]. Earthworms are rare in the SNP and therefore were not included. We collected eight random 2.2 cm diameter x 10 cm deep soil cores from each plot in September 2013 to determine the soil nematode community composition. The samples were mixed and the nematodes were extracted from 100 ml of fresh soil using Oostenbrink elutriators (Oostenbrink 1960). All nematodes in a 1 ml of the 10 ml extract were counted, a minimum of 150 individuals sample-1 were identified to genus or family level using (Bongers 1988), the numbers of all nematodes were extrapolated to the entire sample and expressed for a 100 g dry sample. In total we identified 63 genus or family levels (Vandegehuchte and others 2015). The list of all the nematodes found is published (Vandegehuchte and others 2015) [http://www.oikosjournal.org/appendix/oik-03341] or DOI: [doi: 10.1111/oik.03341].
We are aware that sampling soil microbes from 2009 to 2011 and soil arthropods in 2011 was not ideal, but we are positive that this does not bias the results. Most of the parameters measured in our experiment either already showed a treatment response after the first growing season (e.g., plant biomass) or did not respond over the entire time experiment (e.g., microbial biomass C). The microbial community composition (2009 – 2011) was highly influenced by inter-annual differences in temperature and precipitation, but did not differ between treatments or vegetation types (Hodel and others 2014). We therefore felt comfortable using the 2009 through 2011 data for describing the soil microbial community in our experimental treatments. Similarly, we are positive that our soil arthropod data are representative. We did assess soil arthropods in August 2012 and found no differences to the August 2011 data. However, we did not feel comfortable combining the 2011 June, July, August data with only August data for 2012 for our analyses.
Sampling of soil properties
We collected three soil samples (5 cm diameter x 10 cm depth) in each plot in September 2013 after removing the vegetation. First, we collected the top layer of mineral soil rich in organic matter, the surface organic layer or rhizosphere, typically 1 to 3 cm in depth with a soil corer (AMS Samples, American Falls, Idaho, USA). Second, we collected a 10 cm mineral soil core beneath this surface layer. The cores for each layer were composited, dried at 65 °C for 48 h and fine-ground to pass a 0.5 mm screen. We then analysed all samples for total C using a Leco TruSpec Analyser (Leco, St. Joseph, Michigan, USA). Mineral soil pH was measured potentiometrically in 1:2 soil:CaCl2 solution with an equilibration time of 30 min.
Soil net N mineralisation was assessed during the 2013 growing season (Risch and others 2015). For this purpose, we randomly collected a 5 cm diameter x10 cm deep soil sample with a soil corer (AMS Samples, American Falls, Idaho, USA) after clipping the vegetation in June 2013. After weighing and sieving (4 mm mesh) the soil, we extracted a 20 g subsample in 1 mol l-1 KCl for 1.5 h on an end-over-end shaker and thereafter filtered it through ashless folded filter paper (DF 5895 150, ALBET LabScience, Hahnenmühle FineArt GmbH, Dassel, Germany). From these filtrates NO3- concentrations were measured colorimetrically (Norman and Stucki 1981) and NH4+with flow injection analysis (FIAS 300, Perkin Elmer, Waltham Massachusetts, USA) (Risch and others 2015). We dried the rest of the sample 105 °C to constant mass to determine fine,fraction bulk density. A second soil sample was collected within each plot in June 2013 with a corer lined with a 5 x 13 cm aluminium cylinder. The corer was driven 11.5 cm deep into the soil so that the top 1.5 cm of the cylinder remained empty. Into this space we placed a polyester bag (250 µm) filled an ion-exchanger resin to capture the incoming N. The bag was filled with a 1:1 mixture of acidic and alkaline exchanger resin (ion-exchanger I KA/ion exchanger IIIAA, Merck AG, Darmstadt, Germany). We then removed 1.5 cm soil at the bottom of the cylinder and placed a second resin exchanger bag into this space to capture the N leached from the soil column. To assure that the exchange resin was saturated with H+ and Cl- prior to filling the bags, the mixture was stirred with 1.2 ml l-1 HCl for 1 h and then rinsed with demineralized water until the electrical conductivity of the water reached 5 µm cm-1. The cylinder with the resin bags in place was reinserted into the soil with the top flush to the soil surface and incubated for three months. We recollected the cylinders in September 2013. Each resin bag and 20 g of sieved soil (4 mm mesh) from each cylinder were then separately extracted with KCl and NO3- and NH4+ concentrations were measured. Nitrate and NH4+ concentrations of all samples were then converted to a content basis by multiplying their values with fine fraction bulk density. Net N mineralisation was thereafter calculated as the difference between the N content of the samples collected at the end of the three-month incubation (including the N extracted from the bottom resin bag) and the N content at the beginning of the incubation (Risch and others 2015).
Soil CO2 emissions were measured every two weeks between 0900 and 1700 hrs from early May through late September 2013 with a PP-Systems SRC-1 soil respiration chamber (15 cm high, 10 cm diameter; closed circuit) attached to a PP-Systems EGM-4 infrared gas analyser (PP-Systems, Amesbury, MA, USA) on two locations per plot (Risch and others 2013). The chamber was placed on randomly placed, permanently installed PVC collars (10 cm diameter) driven 5 cm into the soil at the beginning of the study (Risch and others 2013). Freshly germinated plants growing within the collars were removed prior to each measurement to avoid measuring plant respiration or photosynthesis. The two measurements collected per plot and sampling date were averaged.
Soil moisture (with time domain reflectometry; Field-Scout TDR-100, Spectrum Technologies, Plainfield, Illionois, USA) and temperature (with a waterproof digital pocket thermometer; Barnstead International, Dubuque, Iowa, USA) were measured at five random locations per plot every two weeks during the growing seasons during the experiment for the 0 to 10 cm depth (Risch and others 2013, 2015). As soil moisture and soil temperature were highly negatively correlated (Risch and others 2013), we only used soil moisture for this study. We used plot-level averages of all values available to capture soil moisture variability during the five years of the experiment. The results remained unchanged when we only used soil moisture from the 2013 growing season.
Numeral calculations and statistical analyses
Ecosystem coupling. We conducted principal component analyses (PCAs; unscaled) at the complete dataset level using the abundances of each taxonomical entity to describe each of the five different communities used in this study: aboveground-dwelling invertebrates, vascular plants, soil microorganisms, soil arthropods and soil nematodes. We retained the first two components (PCA axis 1 and PCA axis 2) of each analysis as we found them to adequately represent the temporal and spatial variability of our 90 treatment plots in previous studies55,67. Together they explained a total of 71.70% of the variation for aboveground invertebrates, 44.36% for plants, 44.85% for soil microorganisms, 61.85% for soil arthropods and 77.19% for soil nematodes. In addition, we used soil pH and soil organic C content as a proxy for soil chemical properties, soil bulk density as a proxy for soil physical properties and soil moisture (negatively correlated with soil temperature) as a proxy for soil micro-climatic conditions for an overall total of fourteen constituents.
We calculated ecosystem coupling9 for each exclosure treatment within each vegetation type (i.e., 2  5 treatment combinations in total) as an integrated measure of pairwise ecological interactions between ecosystem constituents representing ecological communities and the soil abiotic environment. These ecological interactions are defined by non-parametric Spearman rank correlation analyses between two constituents, excluding interactions involving two abiotic constituents (e.g., soil pH vs. soil moisture) and interactions between the first (PC1) and second (PC2) component of each community type, as these are orthogonal by definition. Interactions between abiotic constituents were excluded from the analyses because the focus of our study was on communities and how they interact with one another and their surrounding environment; therefore, including abiotic-abiotic interactions was not of interest here. Given that the effectiveness of our experimental design resulted in that no community composition data of aboveground-dwelling invertebrates was available for the “None” plots (all animals excluded), only thirteen instead of fourteen constituents were included in the ecosystem coupling calculations for this treatment. The complete absence of aboveground invertebrates represents the most extreme case of disturbance between aboveground animal communities and the rest of the ecosystem constituents. This may have resulted in a slight overestimation of ecosystem coupling for these plots.
	Average ecosystem coupling was calculated as follows:
Ecosystem coupling=
where Xi is the absolute Coupling was calculated value of the Spearman’s rho coefficient of the ith correlation for each treatment within each vegetation type (i.e., based on nine replicates each), considering and n is the number of pairwise comparisons considered (n = a total of 80; interactions (56 in the case of the “None” treatment). We considered a total of 40 biotic-biotic interactions (i.e., concerning two community-level principal components such as plants and microbes; 24 in the case of the “None” treatment) and 40 abiotic-biotic (i.e., concerning one community-level principal component and one abiotic factor, e.g., plant community and soil properties; 32 in the case of the “None” treatment).	Coupling was calculated for each treatment within each vegetation type (i.e., based on nine replicates each), considering a total of 80 interactions (56 in the case of the “None” treatment). We considered a total of 40 biotic-biotic interactions (i.e., concerning two community-level principal components such as plants and microbes; 24 in the case of the “None” treatment) and 40 abiotic-biotic (i.e., concerning one community-level principal component and one abiotic factor, e.g., plant community and soil properties; 32 in the case of the “None” treatment).
To establish whether constituents were significantly and positively coupled within treatments (i.e., the average of their correlation coefficients were greater than in a null model where correlation only happens by chance), we calculated one-tailed p-values based on permutation tests with 999 permutations.

We considered six ecosystem functions and process rates commonly used to assess ecosystem functioning (Meyer and others 2015; Manning and others 2018). Plant N content represents a measure of forage quality, while plant richness has been shown to stabilise biomass production, thus allowing the system to respond to changes in herbivory. Soil net N mineralisation, soil respiration, root biomass, and microbial biomass represent fluxes or stocks of energy. For all functions and processes higher values represent higher functioning (Manning and others 2018). All these variables were measured in the last year of the experiment (2013). We then quantified ecosystem multifunctionality using the multiple threshold approach (Byrnes and others 2014; Manning and others 2018), which considers the number of functions that are above a certain threshold, over a series of threshold values (typically 10-99%) that are defined based on the maximum value of each function. We weighted all our functions equally for these calculations (Manning and others 2018). The number of functions in a plot with values higher than a given threshold value for the respective function is summed up. The sum represents ecosystem multifunctionality for that plot. Given that choosing any particular threshold as a measure of ecosystem multifunctionality is arbitrary, we calculated the average of thresholds from 10-90% (in 10% intervals) as a more integrated representation of ecosystem multifunctionality.
We used Pearson correlations to explore the relationships between ecosystem coupling (all interactions, biotic-biotic interactions, abiotic-biotic interactions involving above- and belowground constituents, and all interactions, biotic-biotic interactions, abiotic-biotic interactions involving belowground constituents only) and ecosystem multifunctionality by calculating the slopes of all relationships between ecosystem coupling and multifunctionality for all thresholds between 10 and 99%. We also related ecosystem coupling with the average of multifunctionality at thresholds between 30-80% as explained before and considered this correlation as a robust indication of the type of association between these two variables. In addition, we explored the relationships between ecosystem coupling (all interactions, biotic-biotic interactions, abiotic-biotic interactions involving above- and belowground constituents, and all interactions, biotic-biotic interactions, abiotic-biotic interactions involving belowground constituents only) and individual ecosystem functions. The effects of exclosures and vegetation type on individual functions and multifunctionality were evaluated using linear mixed effects models ('lme' function of the nlme package), with exclosure and vegetation type as fixed effects and fence as a random factor. All statistical analyses and numerical calculations were done in R version 3.4.0 (R Core Team 2016).

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- Oostenbrink M. 1960. Estimating nematode populations by some selected methods. In: Sasser NJ, Jenkins WR, editors. Nematology. Chapel Hill, NC, USA: University of North Carolina Press. pp 85–101.
- R Core Team. 2016. R: A language and environment for statistical computing. Vienna, Austria: R Foundation for Statistical Computing
- Risch AC, Haynes AG, Busse MD, Filli F, Schütz M. 2013. The response of soil CO2 fluxes to progressively excluding vertebrate and invertebrate herbivores depends on ecosystem type. Ecosystems 16:1192–202.
- Risch AC, Schütz M, Vandegehuchte ML, Van Der Putten WH, Duyts H, Raschein U, Gwiazdowicz DJ, Busse MD, Page-Dumroese DS, Zimmermann S. 2015. Aboveground vertebrate and invertebrate herbivore impact on net N mineralization in subalpine grasslands. Ecology 96:3312–22.
- Schütz M, Risch AC, Achermann G, Thiel-Egenter C, Page-Dumroese DS, Jurgensen MF, Edwards PJ. 2006. Phosphorus translocation by red deer on a subalpine grassland in the Central European Alps. Ecosystems 9:624–633.
- Schütz M, Risch AC, Leuzinger E, Krüsi BO, Achermann G. 2003. Impact of herbivory by red deer (Cervus elaphus L.) on patterns and processes in subalpine grasslands in the Swiss National Park. For Ecol Manage 181:177–88.
- Vandegehuchte ML, van der Putten WH, Duyts H, Schütz M, Risch AC. 2017a. Aboveground mammal and invertebrate exclusions cause consistent changes in soil food webs of two subalpine grassland types, but mechanisms are system-speciﬁc. Oikos 126:212–23.
- Vandegehuchte ML, Raschein U, Schütz M, Gwiazdowicz DJ, Risch AC. 2015. Indirect short- and long-term effects of aboveground invertebrate and vertebrate herbivores on soil microarthropod communities. PLoS One 10:e0118679.
- Vandegehuchte ML, Schütz M, de Schaetzen F, Risch AC. 2017b. Mammal-induced trophic cascades in invertebrate food webs are modulated by grazing intensity in subalpine grassland. J Anim Ecol 86:1434–46.
- Vandegehuchte ML, Trivellone V, Schütz M, Firn J, de Schaetzen F, Risch AC. 2018. Mammalian herbivores affect leafhoppers associated with specific plant functional types at different timescales. Funct Ecol 32:545–55.
- Wirthner S, Frey B, Busse MD, Schütz M, Risch AC. 2011. Effects of wild boar (Sus scrofa L.) rooting on the bacterial community structure in mixed-hardwood forest soils in Switzerland. Eur J Soil Biol 47:296–302. http://dx.doi.org/10.1016/j.ejsobi.2011.07.003
- Zumsteg A, Luster J, Göransson H, Smittenberg RH, Brunner I, Bernasconi SM, Zeyer J, Frey B. 2012. Bacterial, Archaeal and Fungal Succession in the Forefield of a Receding Glacier. Microb Ecol 63:552–64. https://doi.org/10.1007/s00248-011-9991-8

ecosystem-coupling

display_name: ecosystem-coupling

ecosystem-functions

display_name: ecosystem-functions

ecosystem-multifunctionality

display_name: ecosystem-multifunctionality

exclusion

display_name: exclusion

grassland

display_name: grassland

grazing

display_name: grazing

invertebrates

display_name: invertebrates

swiss-national-park

display_name: swiss-national-park

vertebrates

display_name: vertebrates

en: Ecosystem coupling and multifunctionality - exclosure experiment


en: orography glaciers paleo-climate precipitation air-temperature last-glacial-maximum

en: Technical documentation

en: Technical documentation containing file metadata and variable descriptions.

en: Data Access

en:
High resolution, downscaled climate model data are used in a wide variety of applications in environmental sciences. Here we present the CHELSA-TraCE21k downscaling algorithm to create global monthly climatologies for temperature and precipitation at 30 arcsec spatial resolution in 100 year time steps for the last 21,000 years. Paleo orography at high spatial resolution and at each timestep is created by combining high resolution information on glacial cover from current and Last Glacial Maximum (LGM) glacier databases with the interpolation of a dynamic ice sheet model (ICE6G) and a coupling to mean annual temperatures from CCSM3-TraCE21k. Based on the reconstructed paleo orography, mean annual temperature and precipitation was downscaled using the CHELSA V1.2 algorithm.

The data is published under a Creative Commons Attribution 2.0 Generic (CC BY 2.0) license.

air-temperature

display_name: air-temperature

glaciers

display_name: glaciers

last-glacial-maximum

display_name: last-glacial-maximum

orography

display_name: orography

paleo-climate

display_name: paleo-climate

en: CHELSA-TraCE21k: Downscaled transient temperature and precipitation data since the last glacial maximum


maintainer: Mountain Hydrology and Mass Movements

en: debris-flow-fatalities ice-avalanche-fatalities flood-fatalities natural-hazard-fatalities earthquake-fatalities landslide-fatalities lightning-fatalities rockfall-fatalities windstorm-fatalities

media_type: text/csv

en: Natural hazard fatalities per year in Swizterland since 1946.

format: CSV

mimetype: text/csv

en:
This dataset contains the number of fatalities due to flood, debris flow, landslide, rockfall, windstorm, lightning, ice avalanche, earthquake and other processes like roof avalanche or lacustrine tsunami for each year since 1946.
The following information is contained (by column and column title):

* year
* total number of hazard fatalities
* number of fatalities by flood (German: Hochwasser, Überschwemmung). Flood includes people drowned in flooded or inundated areas or carried away in streams under high-water conditions.
* number of fatalities by debris flow (German: Murgang).
* number of fatalities by landslide (German: Erdrutsch). Landslide includes people killed by landslides and hillslope debris flows (German: Hangmure).
* number of fatalities by rockfall (German: Steinschlag, Fels- und Bergsturz).
* number of fatalities by windstorm (German: Sturm). Windstorm includes people killed by falling objects or trees during very strong wind conditions and people who drowned in lakes because their boat capsized during such conditions.
* number of fatalities by lightning (German: Blitz).
* number of fatalities by ice avalanche (German: Eislawine).
* number of fatalities by earthquake (German: Erdbeben).
* number of fatalities by other processes like roof avalanche, lacustrine tsunami (German: andere Prozesse wie Dachlawine, Tsunami im See).

The data was collected based on newspaper research. For more information please refer to

_Badoux, A., Andres, N., Techel, F., and Hegg, C.: Natural hazard fatalities in Switzerland from 1946 to 2015, Nat. Hazards Earth Syst. Sci., 16, 2747-2768, https://doi.org/10.5194/nhess-16-2747-2016, 2016._

The data collection is financed by the FOEN (with exception of the collection of the avalanche fatalities). The data contains the official statistics of the FOEN on fatalities due to flood, debris flow, landslide, rock fall and avalanche.

Restrictions: The data set is not complete. Only fatalities in or around settlements and on open transportation routes are included. More precisely, fatalities were not collected, when persons exposed themselves to a great danger on purpose. Or fatalities during leisure activities which are connected to a higher risk were not included (this includes e.g. canoeing or river surfing during flood, canyoning, mountaineering, climbing, walking or driving on a closed road).

Fatalities by avalanches are collected at the WSL Institute for Snow and Avalanche Research SLF. You can download the avalanche fatalities per hydrological year [here](https://www.envidat.ch/dataset/avalanche-fatalities-switzerland-1936) and per calendar year [here](https://www.envidat.ch/dataset/avalanche-fatalities-per-calendar-year-since-1936). For a direct comparison with the fatalities presented here, please download the data set with the calendar years and do not consider fatalities in the backcountry (tour) or in terrain close to ski areas (offpiste).

debris-flow-fatalities

display_name: debris-flow-fatalities

earthquake-fatalities

display_name: earthquake-fatalities

flood-fatalities

display_name: flood-fatalities

ice-avalanche-fatalities

display_name: ice-avalanche-fatalities

landslide-fatalities

display_name: landslide-fatalities

lightning-fatalities

display_name: lightning-fatalities

natural-hazard-fatalities

display_name: natural-hazard-fatalities

rockfall-fatalities

display_name: rockfall-fatalities

windstorm-fatalities

display_name: windstorm-fatalities

en: Number of natural hazard fatalities per year in Switzerland since 1946


maintainer: Dirk Nikolaus Karger

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

en: CHELSA Technical Documentation

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

en: CHELSA V2.1 (current)

en: CHELSA Version 2.1 based on ERA5 forcings and CMIP6

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

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.


maintainer: Yael Frischholz

en: alpine renewable-energy snow-transport photovoltaic preferential-deposition

en: Browse simulation files

en:
This file contains the snowBedFoam simulations carried out to produce the results presented in: _article not published yet_.
 Content
 1. /simulations
Groups all simulations folders organised by parameter (azimuth, groupsize, height, interspace) and by type of experiment (single_ref, group_ref).
 2. /simulations/[parameter]/
For each parameter multiple simulations were carried out. Each simulation folder follows the same naming systematic:
`helioplant_n#_h#_ARL#_BL#_az#_windDir#`
- n: number of Helioplant units
- h: height-above-surface
- sp: regular distance between the units
- ARL: additional refinement level
- BL: boundary layer first cell height
- windDir: wind direction
- stag: staggered arangement (suffix)
Here is an example of a folder content for a specific parameter
(simulations/azimuth/):
- `helioplant_n9_h07_sp10_ARL45_BL0015_az30_windDir5`: following the naming systematic this folder corresponds to a simulation with 9 aligned Helioplant units with 0.7m of height-above-surface, an inter-unit distance of 10m an azimuth of 30° and a wind direction of 5°.
 3. /simulations/[parameter]/[helioplant_n#_h#_ARL#_BL#_az#_windDir#]
Each simulation folder contains multiple sub-folders (0/, 100/, 300/, constant/ etc.) and files that define the experiment. For each simulation, the files used in the processing [scripts] are the following:
- 0/Cx: contains the x coordinates of sampling grid cells and of the Helioplants structures.
- 0/Cy: contains the y coordinates of sampling grid cells and of the Helioplants structures.
- 300/kinematicCloud-massCheckPatterns: contains the snow mass distribution values [kg/m2] for each grid cell.

[scripts]: https://github.com/frischwood/snowbed-helio.git

en:
This dataset groups numerical simulation outputs and validation measurement data produced in the context of the following [publication]: _not published yet_
The snow transport model [snowBedFoam] was used to analyse snow deposition around a specific type of Alpine PV structures named HELIOPLANT®.
The results of a sensitivity analysis of multiple key parameters that govern the spatial organisation of these structures are provided here. Measurements of snow distribution taken from the test-site of the [Gondosolar] project, are provided too.

To reproduce the results of the aforementioned publication, follow the instructions on this [repository].
[publication]: https://
[snowBedFoam]: https://www.doi.org/10.16904/envidat.223
[Gondosolar]: https://www.gondosolar.ch
[repository]: https://github.com/frischwood/snowbed-helio.git

alpine

display_name: alpine

photovoltaic

display_name: photovoltaic

preferential-deposition

display_name: preferential-deposition

renewable-energy

display_name: renewable-energy

snow-transport

display_name: snow-transport

en: Drifting and blowing snow distribution around structures for Alpine PV applications


soil-property-maps-for-the-swiss-forest

title_for_slug: soil-property-maps-for-the-swiss-forest

en: soc dsm soil-depth soil-texture soil-properties switzerland soil-ph soil forest

en:
We used 2071 forest soil profiles to model a wide range of soil properties for the forested area of Switzerland. The spatial prediction is based on the principle of «digital soil mapping». This involves linking soil profiles with soil forming factors using statistical or machine learning methods.

A quantile regression forest (QRF) approach was applied to predict the following soil properties at six depth ranges: clay, gravel, sand, fine earth density, SOC. The depth ranges correspond to the standard depths of the [GlobalSoilMap.Net](https://www.isric.org/) specification: 0–5, 5–15, 15–30, 30–60, 60–100 and 100–200 cm. In addition, the total soil depth down to a non-root-permeable layer or solid rock soil thick was predicted. To quantify the uncertainty for each predicted pixel, the upper and lower limit of the 90% prediction interval derived from QRF was calculated. More details on the methods and results are described in Baltensweiler et al. 2021 and Baltensweiler et al 2022.

The soil property maps, and the uncertainty maps are provided as a GeoTIFF files at 25 m resolution. The excel file (xlsx) provides a short description of the raster layers.

**The soil and the uncertainty maps can be viewed in a simple web-GIS application available at:**
[www.wsl.ch/soilmaps](https://www.wsl.ch/soilmaps).

dsm

display_name: dsm

forest

display_name: forest

soc

display_name: soc

soil

display_name: soil

soil-depth

display_name: soil-depth

soil-ph

display_name: soil-ph

soil-properties

display_name: soil-properties

soil-texture

display_name: soil-texture

switzerland

display_name: switzerland

en: Soil property maps for the Swiss forest


en: urban-ecosystems honeybees dominance cities anthophila sads wildbees urban-beekeeping

en: Dataset species abundance

en:
This data resource provides the individual species abundance per city / urban aggregation. It contains data from 41 datasets from 37 studies collected in 33 cities / urban aggregations. It contains the following columns:
 - Article_ID
- DOI
- Authors
- Year
- Continent
- Country
- City
- Bee genus
- Bee species
- Bee merged
- Bee full
- Abundance
- Bee_ID_per_study: ID for the study

en: Dataset proportion honeybees and wild bees

en:
The dataset provide the main features for each included dataset from published and unpublished research works. Each row represents a dataset, which provides bee community data in one city / urban aggregation. Overall, it contains 68 datasets from 46 cities in 15 countries and five continents. The data is organised in the following columns:
- Article_ID: id used in the study
- DOI: doi of the publication, when available
- Authors
- Year: of publication
- Duration sampling (years)
- Start_sampling: month of the year
- End_sampling: month of the year
- Continent
- Country
- N. cities: number of cities included in the publication
- City
- Sampling type: active, passive or both
- Sampling methodology: within each sampling type.
- Habitats: list of sampling habitats
- N_habitats: number of sampling habitats
- Parks_similar: binnary (1 = yes; 0 = no)
- Agriculture: binnary (1 = yes; 0 = no)
- Private_gardens: binnary (1 = yes; 0 = no)
- Green_roofs: binnary (1 = yes; 0 = no)
- seminatural_natural_wasteland: binnary (1 = yes; 0 = no)
- other_unspecified: binnary (1 = yes; 0 = no)
- Number sites
- Abundance honeybees
- Abundance wild bees
- Total bees
- Proportion honeybees
- Proportion wildbees
- Area:. of the studied city/urban aggregation

en: Dataset coordinates study cities

en:
The data contains the latitude and longitude of the studied cities / urban aggregations. It contains the following columns:
- Continent
-Country
- City
- Lat: Latitude
- Lon: Longitude

en: R script for analyses and plots

format: OCTET

en:
The following repository contains the data and code to reproduce the figures analyses of the paper "Examining honeybee (Apis mellifera) dominance patterns within urban bee communities worldwide". It contains three datasets and one .R file

---

The data results from a literature review on abundance distribution of urban bee communities worldwide, aiming at obtaining studies reporting total abundances of honeybees and wildbees in a given city, and species abundances of wildbees and honeybees in a given city.

---

1. **Data**:
- *20240308_cities_coords.csv*: the data contains the latitude and longitude of the included cities in the study. It is used for making the world map with the cities.
- *20241201_proportion_HB_WB.csv*: the data contains the total wild bee and honeybee abundances per city/urban aggregation, and the proportions.
- *20241201_rad_bees.csv*: the data contains the species abundances per city/urban aggregation

2. **Script**:
- *HoneybeeDominance_Analyses_Figures.R*: the script to run the analyses and make the plots. Analyses were done in R version 4.2.1, using the packages ggplot2, glmmTMB, multcomp, wesanderson, terra.

anthophila

display_name: anthophila

cities

display_name: cities

dominance

display_name: dominance

honeybees

display_name: honeybees

sads

display_name: sads

urban-beekeeping

display_name: urban-beekeeping

urban-ecosystems

display_name: urban-ecosystems

wildbees

display_name: wildbees

en: Data supporting ‘Examining honeybee (Apis mellifera) dominance patterns within urban bee communities worldwide’


urban-birds-point-counts-data

title_for_slug: urban-birds-point-counts-data

en: biodiversity urban environmental-gradients spatially-distributed-sampling periurban birds

en:
The study area included the cities of Basel, Lugano and Zurich. The sampling design reflected four main city districts related to four categories of tree cover (Figure 1): 1) industrial/commercial areas, 0-20% tree cover; 2) residential areas, 20-40% tree cover; 3) urban parks and cemeteries, 40-60% tree cover; 4) peri-urban forests (natural/semi-natural forests), 60-100% tree cover. The tree cover gradient was evaluated across a square grid with a square side length of 100 m. For each square, we evaluated the area covered by urban trees using the Urban Atlas Street Tree Layer 2018 (European Union’s Copernicus Land Monitoring Service information, 2021).
In each city, we established eight transects of 1.2 km, two for each tree cover category. Transects crossed contiguous grid squares belonging to the same tree cover categories as much as possible. We performed aural-visual point counts of birds every 200 m along each transect (six points per transect) during the breeding season (April-June 2024) (Bibby et al., 2000). The transects were walked at the time of highest activity of birds, which is from thirty minutes after sunrise until 4 hours later. Each transect was walked twice, 20-60 days apart, to account for imperfect detection of birds and sample completeness (Balestrieri et al., 2017; Kéry et al., 2005).

biodiversity

display_name: biodiversity

birds

display_name: birds

environmental-gradients

display_name: environmental-gradients

periurban

display_name: periurban

spatially-distributed-sampling

display_name: spatially-distributed-sampling

urban

display_name: urban

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: Urban birds point counts data


maintainer: Michael Nobis

en: artificial-intelligence invasive-species computer-vision automatic-detection plants biological-invasions

en: Detected occurrences of Ailanthus altissima along highways on the Swiss Plateau. The number of image tiles in which the species was recognized is shown (Fig. 23 in the report). Image coordinates of the middle and side strips can be displayed separately in the interactive map.

en: Detected occurrences of Senecio inaequidens along highways on the Swiss Plateau. To reduce false-positives, only images in which the species was recognized in at least three of 16 image tiles are considered as occurrences (Fig. 40 in the report). Image coordinates of the middle and side strips can be displayed separately in the interactive map.

en: Detected occurrences of Ailanthus altissima along highways on the Swiss Plateau. To reduce false-positives, only images in which the species was recognized in at least three of 16 image tiles are considered as occurrences (Fig. 38 in the report). Image coordinates of the middle and side strips can be displayed separately in the interactive map.

en: Detected occurrences of Senecio inaequidens along highways on the Swiss Plateau. The number of image tiles in which the species was recognized is shown (Fig. 25 in the report). Image coordinates of the middle and side strips can be displayed separately in the interactive map.

en:
Transport infrastructure such as **highways** are important corridors for the spread of invasive species. In this project, an automated detection and mapping of **two invasive alien plant species** was developed and applied along highways in the **Swiss Central Plateau**, based on **artificial intelligence (AI, Deep Learning)**. The two target species are **tree of heaven *(Ailanthus altissima)*** and **narrow-leaved ragwort *(Senecio inaequidens)***.
The data is part of the project report and shows the mapping results in **interactive maps**. Technically speaking, these are **self-contained HTML files** that can be displayed with standard web browsers. To reduce the file size, the downloads are provided in zip format.
**Report**: [https://www.mobilityplatform.ch/de/research-data-shop/product/1690](https://www.mobilityplatform.ch/de/research-data-shop/product/1690)
**Project**: [https://www.wsl.ch/en/projects/automated-detection-of-invasive-alien-plants-along-highways/](https://www.wsl.ch/en/projects/automated-detection-of-invasive-alien-plants-along-highways/)

artificial-intelligence

display_name: artificial-intelligence

automatic-detection

display_name: automatic-detection

biological-invasions

display_name: biological-invasions

computer-vision

display_name: computer-vision

invasive-species

display_name: invasive-species

plants

display_name: plants

en: Automated detection of invasive alien plants along highways


maintainer: Peter Bebi

en: stillberg soil-temperature climate-change experiment vegetation carbon-dioxide

en: Project Description FACE Stillberg

media_type: text/html

en: Link to FACE project description on the WSL website.

format: HTML

en: Data FACE Stillberg

en: Folder in .zip format containing the FACE datasets.

en: Metadata FACE Stillberg Data File Description

en: List of descriptions for each of the .csv FACE data files.

en: Metadata FACE Stillberg Experimental Design

en: Schematic illustration and tabular listing of the FACE experimental design.

en:
 Background information

High elevation ecosystems are important in research about environmental change because shifts in climate associated with anthropogenic greenhouse gas emissions are predicted to be more pronounced in these areas compared to most other regions of the world. This project involved a Free Air CO2 Enrichment (FACE) and soil warming experiment located in a natural treeline environment near Davos, Switzerland (Stillberg, 2200 m a.s.l.). Elevated atmospheric CO2 concentrations (+200 ppm) were applied from 2001 until 2009, and a soil warming treatment (+4 °C) was applied from 2007 until 2012. The combined CO2 enrichment and warming treatment reflects conditions expected to occur in this region in approximately 2050. A broad range of ecological and biogeochemical research was carried out as part of this environmental change project.

 Experimental design

The experiment consisted of 40 hexagonal 1.1 m² plots, 20 with a *Pinus mugo* ssp. *uncinata* (mountain pine, evergreen) individual in the centre and 20 with a *Larix decidua* (European larch, deciduous) individual in the centre. A dense cover of understorey vegetation surrounded the tree in each plot, including the dominant dwarf shrub species *Vaccinium myrtillus* (bilberry), *Vaccinium gaultherioides* (group *V. uliginosum agg.*, northern bilberry) and *Empetrum nigrum* ssp. *hermaphroditum* (crowberry) plus several herbaceous and non-vascular species.
At the beginning of the experimental period, the 40 plots were assigned to ten groups of four neighbouring plots (two larch and two pine trees per group) in order to facilitate the logistics of CO2 distribution and regulation. Half of these groups were randomly assigned to an elevated CO2 treatment, while the remaining groups served as controls and received no additional CO2. In spring 2007, one plot of each tree species identity was randomly selected from each of the 10 CO2 treatment groups and assigned a soil warming treatment, yielding a balanced design with a replication of five individual plots for each combination of CO2 level, warming treatment and tree species.

 Data description

Soil and air conditions have been monitored closely throughout the study period, with most measurements made during the combined CO2 x warming experiment (2007-2009). The data comprise of air temperature, soil temperature, soil moisture, sapflow, tree diameter and CO2 measurements.

carbon-dioxide

display_name: carbon-dioxide

climate-change

display_name: climate-change

experiment

display_name: experiment

soil-temperature

display_name: soil-temperature

stillberg

display_name: stillberg

vegetation

display_name: vegetation

en: FACE: Stillberg CO2 enrichment and soil warming study


maintainer: Adam Winstral

en: jim jules-investigation-model snow-depth snow snow-simulation

en: Station forcing data

en: All forcing data need to run JIM at HS and SWE stations. These are data downscaled directly from COSMO NWP data (WY14, WY15) and further enhanced by additional station observations of snow depth (HS) and air temperature (Ta) in WY17. Further information can be found in README file. Note that in WY14 and WY15, shortwave radiation was not split into direct and diffuse (not necessary for JIM) and that the default method in JIM for splitting precipitation phase was used. In WY 17, direct and diffuse were combined as input to JIM and JIM was forced with pre-processed liquid and solid precipitation phases.

en: HS and SWE observations

en: Automated (HS) and manual (SWE) data used to evaluate model simulations

en: DEM

en: 1-km resolution DEM used for downscaling gridded NWP data to stations and for distributing BDE evaluations at HS-stations to SWE-stations

mimetype: text/plain

en: File/data descriptor

en: These data were used to drive and evaluate Jules Investigation Model (JIM) snow simulations. The data provided are the forcing data used for the "deterministic" runs as described in Winstral et al., 2019. The bias-detecting ensemble (Winstral et al., 2019) used observed snow depths (HS) to detect biases in these deterministic simulations related to precipitation and energy inputs to JIM. Simulations that included the BDE evaluations substantially improved JIM simulations.

jim

display_name: jim

jules-investigation-model

display_name: jules-investigation-model

snow

display_name: snow

snow-depth

display_name: snow-depth

snow-simulation

display_name: snow-simulation

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: Meteorological data used to develop and validate the bias-detecting ensemble (BDE)


maintainer: Elisabeth Hafner

en: satellite avalanche validation avalanche-hazard-mapping snow

en: Satellite Avalanche Mapping Validation data and data description

en: 14 shapefiles to be used only together with the data description also provided as a pdf.

en:
Validation points, validation area, ground truth coverage, SPOT 6 avalanche outlines, Sentinel-1 avalanche outlines, Sentinel-2 avalanche outlines, Davos avalanche mapping (DAvalMap) avalanche outlines as shapefiles and a detailed attribute description (DataDescription_EvalSatMappingMethods.pdf).

Coordinate system: CH1903+_LV95

The generation of this dataset is described in detail in:

Hafner, E. D., Techel, F., Leinss, S., and Bühler, Y.: Mapping avalanches with satellites – evaluation of performance and completeness, The Cryosphere, https://doi.org/10.5194/tc-2020-272, 2021.

avalanche

display_name: avalanche

avalanche-hazard-mapping

display_name: avalanche-hazard-mapping

satellite

display_name: satellite

validation

display_name: validation

en: Satellite avalanche mapping validation data


en: alpine3d lee-side-flow-field preferential-deposition lidar tls

en: Dataset

en:
The data presented here corresponds to the publication "A Close-Ridge Small-Scale Atmospheric Flow Field and its Influence on Snow Accumulation" (Gerber et al., 2017), which investigates an eddy-like structure in the vicinity of the Sattelhorn in the Dischma valley (Davos Switzerland) and its influence on snow accumulation. The dataset contains:

* Alpine3D: Alpine3D snow depth grids (25 m resolution) for two simulations with and without snow redistribution.
* ARPS: 10 ARPS simulations (25 m horizontal resolution) with different model setups (wind direction, wind speed, stability).
* LiDAR: Processed LiDAR PPI (D2_PPI_1h) and RHI (D2_cross_1h) across the valley with a hourly resolution for the period 27 October 2015 01:00 - 29 October 2015c 21:00 (spatial resolution: 25 m).
* meteostations-dischma: Meteorological station data of two meteorological stations in the Dischma valley with 10 minute resolution for the period 28 October 2015 - 30 October 2015.
* TLS: Snow depth change data (m) between 28 October 2015 and 30 October 2015 based on terrestrial laser scans.

For more details about the simulation and observation data, see Gerber et al., 2017.

Publication: Gerber et al., 2017: A Close-Ridge Small-Scale Atmospheric Flow Field and its Influence on Snow Accumulation, submitted to JGR - Atmospheres.

lee-side-flow-field

display_name: lee-side-flow-field

lidar

display_name: lidar

preferential-deposition

display_name: preferential-deposition

tls

display_name: tls

en: DISCHMEX - Observations and simulations of the close-ridge small-scale atmospheric flow field and snow accumulation at Sattelhorn, Dischma valley, Davos, Switzerland.