en:
The data correspond to the experiments presented and discussed in a paper regarding the interaction between turbulent wind fluctuations and snow saltation mass-fluxes (Paterna, 2016). Each of the nine data files corresponds to a different experiment presented in the paper and conducted in the winter 2014/2015 in the WSL/SLF cold wind tunnel in Davos. For each file the five columns indicate the time from the beginning of the experiment, the streamwise (u’) and the vertical (w’) wind velocity fluctuations, the streamwise (qx) and the vertical (qz) snow mass-flux components. From these time-series the scales of the snow saltation and of the turbulent flow are obtained with respect to the eddy-cycles and snow saltation cycles. From spectral analysis of the time-series a decoupling of the snow saltation from the turbulence forcing reveals two regimes of interaction: a turbulence-dependent regime occurring with weak saltation, and a turbulence-independent regime with strong saltation. Further details can be found at the link below.

Publication http://onlinelibrary.wiley.com/doi/10.1002/2016GL068171/abstract

en: boundary-layer-winds saltation snow-cover snow-depth vertical-wind-motion

en: Wind tunnel measurement data of drifting snow and turbulent wind fluctuations

en: Compressed TXT files

en: Data Compilation

boundary-layer-winds

display_name: boundary-layer-winds

saltation

display_name: saltation

snow-cover

display_name: snow-cover

snow-depth

display_name: snow-depth

vertical-wind-motion

display_name: vertical-wind-motion


$oid: OBSOLETE

en:
This dataset contains eddy-covariance measurements in the ablation period of 2014-2016. Measurements were taken from two turbulence towers over a long-lasting snow patch, which are 5 m apart from each other (2014 and 2015). The turbulence towers were equipped with two YOUNG ultrasonic anemometers mounted 0.7 m (in 2014) and 3.3 m (in 2015) above snow-free ground, two ultrasonic anemometers (CSAT3, Campbell Scientific, Inc.) mounted at 2.6 m (in 2014) and 2.2 m (in 2015) above snow-free ground and one anemometer (DA-600, Kaijo Denki) mounted at 0.3 m above snow surface.

The measurement setup changed in 2016 and includes a measurement above the snow-free ground in upwind direction (Swiss coordinates: 790191/176689). The measurement tower is equipped with one ultrasonic anemometer (CSAT3, Campbell Scientific, Inc.) in 3.3 m above the snow-free ground. Additionally, one measurement tower is installed above the long-Lasting snow patch and equipped with the same setup as 2015.

Turbulence data were sampled at a frequency of 20 Hz. The processing of the data to quality controlled fluxes has been done with the Biomicrometeorology flux software (Thomas et al., 2009). The program applies plausibility tests and a despiking test after Vickers and Mahrt (1997) on the measured data. The routine further applies a time-lag correction and considers the deployment (e.g. the sonic azimuth). A frequency response correction (Moore, 1986) is done and a three-dimensional rotation is performed. Finally, quality assurance/quality control (QA/QC) flags after Foken et al., (2004) are issued and fast Fourier transform power and co-spectra are calculated. The change in snow height is considered in the post-processing for every measurement day. The turbulence data were averaged to 30 minute intervals.

en: dischmex eddy-covariance-measurements patchy-snow-covers snow-patch turbulent-sensible-heat-fluxes

envidat

approval_status: approved

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.

de: EnviDat: das Umwelt-Datenportal

en: EnviDat: the Environmental Data Portal

fr: EnviDat: le portail de données environnementales

it: EnviDat: il portale dei dati ambientali

political_level: other

state: active

type: organization

wsl

capacity: public

en: DISCHMEX - Impact of extreme land-surface heterogeneity on micrometeorology over spring snow-cover

type: dataset

key: guid

key: uri

value: Envidat Harvester

educ

de: Bildung, Kultur und Sport

en: Education, culture and sport

fr: Éducation, culture et sport

it: Istruzione, cultura e sport

en: Eddy-covariance measurement with an ultrasonic anemometer (CSAT3, Campbell Scientific, Inc.) in 2.6 m.

format: ZIP

media_type: application/zip

en: Eddy-covariance measurement with an ultrasonic anemometer (R.M. Young Company) in 0.7 m.

en: Eddy-covariance measurement with an ultrasonic anemometer (DA-600, Kaijo-Denki) in 0.3 m on a daily basis.

en: Eddy-covariance measurement with an ultrasonic anemometer (CSAT3, Campbell Scientific, Inc.) in 2.2 m.

en: Eddy-covariance measurement with an ultrasonic anemometer (R.M. Young Company) in 3.3 m.

en: Eddy-covariance measurement with an ultrasonic anemometer (R.M. Young Company) in 3.5 m.

en: Eddy-covariance measurement with an ultrasonic anemometer (CSAT3, Campbell Scientific Inc.) in 3.2 m on a daily basis.

en: Eddy-covariance measurement with an ultrasonic anemometer (CSAT3, Campbell Scientific Inc.) in 1.7 m on a daily basis.

en: Output explanation

format: XLS

en: Background map based on data © 2014/2016 swisstopo (JD100042)

en: Gletschboden setup

format: PNG

media_type: image/png

dischmex

display_name: dischmex

eddy-covariance-measurements

display_name: eddy-covariance-measurements

patchy-snow-covers

display_name: patchy-snow-covers

snow-patch

display_name: snow-patch

turbulent-sensible-heat-fluxes

display_name: turbulent-sensible-heat-fluxes


en:
Dataset of meteorological and snowpack measurements from the automatic weather station at Weissfluhjoch, Davos, Switzerland, suitable for driving snowpack models. The dataset contains standard meteorological measurements, and additionally snowpack runoff data from a snow lysimeter. Where possible, data is quality checked and missing data are replaced from backup sensors from the measurement site itself, or (in only a few cases) from the MeteoSwiss weather station at 470 m distance and 150 m above the measurement site.

Publication
Wever, N., Schmid, L., Heilig, A., Eisen, O., Fierz, C., and Lehning, M. Verification of the multi-layer SNOWPACK model with different water transport schemes. 2015. The Cryosphere. Volume 9. 2271-2293. http://dx.doi.org/10.5194/tc-9-2271-2015.

en: air-temperature humidity longwave-radiation precipitation-amount shortwave-radiation snow-depth snow-ice-temperature wind-direction wind-speed

en: WFJ_MOD: Meteorological and snowpack measurements from Weissfluhjoch, Davos, Switzerland

en:
Release notes:

Bug fix: in previous versions, snow lysimeter data from September 2010 onwards was erroneously reported for UTC+2, instead of UTC+1 (i.e., reported one hour later than should have been).

Update: dataset extended to 2017-07-11T00:30.

en: Version 7 (current)

format: SERVICE

en: This ini-file can be used to run SNOWPACK simulations with the WFJ data set, using the new MeteoIO Filter, Generator and Interpolation syntax.

en: SNOWPACK ini file (new syntax)

en: This ini-file can be used to run SNOWPACK simulations with the WFJ data set, using version 3.4.0 or higher.

en: SNOWPACK ini file (old syntax)

en: This sno-file can be used to run SNOWPACK simulations with the WFJ data set, using version 3.4.0 or higher.

en: SNOWPACK sno file

en: This document describes how the undercatch correction for the Weissfluhjoch measurement site was determined.

en: Undercatch correction

format: PDF

media_type: application/pdf

en:
Deprecated version.

Release notes:

- Missing ISWR for 2009-09-30 and 2010-04-30 has been replaced by data from WFJ Gipfel

This dataset is the basis for the Weissfluhjoch dataset in ESM-SnowMIP (doi: http://dx.doi.org/10.16904/16).

en: Version 6

en:
Deprecated version. Release notes:

Update: using the incoming and outgoing short- and longwave radiation data from the new processing chain from 2010 onwards, filling also data gaps in pre-2010 data.

Update: dataset extended to 2016-10-04T00:30

Update: refreshing data originating from MeteoSwiss (particularly precipitation)

en: Version 5

en:
Deprecated version. Release notes:

Update: dataset extended to 2016-09-02T00:30

Update: refreshing data originating from MeteoSwiss (particularly precipitation)

en: Version 4

en:
Deprecated version. Release notes:

Bug fix: in version 2, the undercatch correction was not applied correctly

Bug fix: in version 2, snow lysimeter data was missing for extended periods of time

Update: dataset extended to 2016-01-02T00:30

Update: refreshing data originating from MeteoSwiss (particularly precipitation)

en: Version 3

en:
Deprecated version. Release notes:

Bug fix: in v1, incoming radiation components were taken from WFJ_Gipfel station, instead of WFJ Versuchsfeld.

en: Version 2

en:
Deprecated version. Release notes:

First release of dataset.

en: Version 1

en: All versions

air-temperature

display_name: air-temperature

humidity

display_name: humidity

longwave-radiation

display_name: longwave-radiation

precipitation-amount

display_name: precipitation-amount

shortwave-radiation

display_name: shortwave-radiation

snow-ice-temperature

display_name: snow-ice-temperature


en:
Stable water isotopes (δ18O) obtained from snow and ice samples of polar regions are used to reconstruct past climate variability, but heat and mass transport processes can affect the isotopic composition. Here we present an experimental study on the effect on the snow isotopic composition by airflow through a snow pack in controlled laboratory conditions. The influence of isothermal and controlled temperature gradient conditions on the δ18O content in the snow and interstitial water vapor is elucidated. The observed disequilibrium between snow and vapor isotopes led to exchange of isotopes between snow and vapor under non-equilibrium processes, significantly changing the δ18O content of the snow. The type of metamorphism of the snow had a significant influence on this process.
Ebner, P. P., Steen-Larsen, H. C., Stenni, B., Schneebeli, M., and Steinfeld, A.: Experimental observation of transient δ18O interaction between snow and advective airflow under various temperature gradient conditions, The Cryosphere Discuss., https://doi.org/10.5194/tc-2017-16, accepted, 2017.

en: advection metamorphism snow stable-water-isotope 18o

envidat

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

en: EnviDat: the Environmental Data Portal

en: Experiments on stable water isotopes,  snow metamorphism, and advection

educ

en: Education, culture and sport

en: A short description of the data contained in the zipped-file. Recommended for reading before downloading the dataset.

en: Read-me

format: TXT

media_type: text/plain

en: raw data and micro-CT data available from contacts

en: Data files and read-me

advection

display_name: advection

metamorphism

display_name: metamorphism

snow

display_name: snow

stable-water-isotope

display_name: stable-water-isotope


en: We recorded snow ablation maps with a terrestrial laser scanner (TLS, Riegl-VZ6000) at the Gletschboden area. The TLS position is located approximately 30 vertical meters above the Gletschboden area at a northerly exposed slope. In total 44 TLS measurement sets have been conducted in three consecutive years 2014-2016 (2014: 13 measurements; 2015: 17 measurements; 2016: 14 measurements). The TLS system has a single-point measurement frequency of 300 kHz and a beam divergence of 0.007°. This set-up allows a horizontal resolution of approximately 0.01 m in 100 m distance to the TLS position. One scan of the Gletschboden area lasts approximately 15 minutes. The travel time from the laser scanner towards the surface is recorded and afterwards converted into a point cloud of distances. 5 reflectors located at the Gletschboden area and in the closer surroundings were additionally scanned during each measurement to transform the point cloud from the scanner own coordinate system into Swiss coordinates. Additionally, orthophotos have been created by using pictures recorded from the TLS in order to provide snow mask maps. Snow and bare ground can be distinguished by the RGB color information of the orthophoto. Cells with blue band information greater than 175 were categorized as snow and all cells with values smaller or equal 175 were categorized as bare ground.

en: patchy-snow-covers riegl-vz6000 snow-ablation-rates terrestrial-laser-scanning tls

en: DISCHMEX - High-resolution daily snow ablation rates in an Alpine environment

en: Digital Elevation Modell 2014

en: Snowmask 2014

en: Digital Elevation Modell 2015

en: Snowmask 2015

en: Digital Elevation Modell 2016

en: Snowmask 2016

en: Gletschboden test site

snow-ablation-rates

display_name: snow-ablation-rates

terrestrial-laser-scanning

display_name: terrestrial-laser-scanning

tls

display_name: tls


weissfluhjoch-dataset-for-esm-snowmip

en: This Weissfluhjoch dataset is a processed version of the Weissfluhjoch dataset version 6 from https://doi.org/10.16904/6. This dataset was specially created for the ESM-SnowMIP project. Here it is documented how this dataset has been created.

en: esm-snowmip snow snow-depth snow-models weissfluhjoch

envidat

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

en: EnviDat: the Environmental Data Portal

en: Weissfluhjoch dataset for ESM-SnowMIP

title_for_slug: weissfluhjoch-dataset-for-esm-snowmip

en: Dataset Weissfluhjoch for ESM-SnowMIP

en:
Use this script to convert WFJ_optimaldataset_v6.smet to wfj.smet, the file that is used for the ESM-SnowMIP project. It also requires the file: WFJ_AirPressure_Data.zip

Use: bash create_wfj_dataset.sh > input/wfj.smet

en: Conversion script

en: This ini file is required by data-converter from MeteoIO version 1887 (http://models.slf.ch/p/meteoio/)

en: ini file

esm-snowmip

display_name: esm-snowmip

snow-depth

display_name: snow-depth

snow-models

display_name: snow-models

weissfluhjoch

display_name: weissfluhjoch


en:
The dataset comprises > 90 000 records from inventories in 54 strict forest reserves in [Switzerland](https://www.wsl.ch/de/wald/biodiversitaet-naturschutz-urwald/naturwaldreservate.html) and [Lower Saxony / Germany](http://naturwaelder.de/) along a considerable environmental gradient. It was used to develop parsimonious, species-specific mortality models for 18 European tree species based on tree size and growth as well as additional covariates on stand structure and climate.

 Inventory data
Measurements had been conducted repeatedly on up to 14 permanent plots per reserve for up to 60 years with re-measurement intervals of 4 - 27 years. The permanent plots vary in size between 0.03 and 3.47 ha. The inventories provide diameter measurements at breast height (DBH) and information on the species and status (alive or dead) of trees with DBH ≥ 4 cm for Switzerland and ≥ 7 cm for Germany.

 Data selection
We excluded three permanent plots where at least 80 % of the trees died during an interval of 10 years, and mortality could be clearly assigned to a disturbance agent. Mortality in the remaining stands was rather low, with a mean annual mortality rate of 1.5 % and strong variation between plots from 0 to 6.5 % (assessed for trees of all species with DBH ≥ 7 cm).
We only used data from permanent plots with at least 20 trees per species to obtain reliable plot-level mortality rates even for species with low mortality rates (about 5 % during 10 years), and selected tree species occurring on at least 10 plots to cover sufficient ecological gradients. This led to a dataset of 197 permanent plots and 18 tree or shrub species: _Abies alba_ Mill., _Acer campestre_ L., _Acer pseudoplatanus_ L., _Alnus incana_ Moench., _Betula pendula_ Roth, _Carpinus betulus_ L., _Cornus mas_ L., _Corylus avellana_ L., _Fagus sylvatica_ L., _Fraxinus excelsior_ L., _Picea abies_ (L.) Karst, _Pinus mugo_ Turra, _Pinus sylvestris_ L., _Quercus pubescens_ Willd., _Quercus_ spp. (_Q. petraea_ Liebl. and _Q. robur_ L.; not properly differentiated in the Swiss inventories), _Sorbus aria_ Crantz, _Tilia cordata_ Mill. and _Ulmus glabra_ Huds..

 Predictors of tree mortality
We considered tree size and growth as key indicators for mortality risk. Radial stem growth between the first and second inventory and DBH at the second inventory were used to predict tree status (alive or dead) at the third inventory. To this end, the annual relative basal area increment (relBAI) was calculated as the compound annual growth rate of the trees basal area. Additional covariates on stand structure and climate comprise mean annual precipitation sum (P), mean annual air temperature (mT), the mean and the interquartile range of DBH (mDBH, iqrDBH), basal area (BA) and the number of trees (N) per hectare.

 Further information
For further information, refer to Hülsmann _et al_. (in press) How to kill a tree – Empirical mortality models for eighteen species and their performance in a dynamic forest model. _Ecological Applications_.

en: empirical-mortality-models forest-reserves inventory-data tree-growth tree-mortality

en: Calibration data for empirical mortality models of 18 European tree species

educ

en: Education, culture and sport

en:
A set of three consecutive inventories was used to generate records for the calibration of mortality models based on trees that were alive in the first and second inventory and either dead or alive in the third inventory.

 Meta data
Reserve: Name of the forest reserve

Plot: Permanent plot number

 Tree data
Species: Latin species name (or species group, cf. _Quercus_ spp.)

y: Status of the tree with 0 = alive and 1 = dead

dt: Length of the mortality period (years)

DBH: Diameter at breast height (mm) of the second inventory

relBAI: Annual relative basal area increment (-) calculated based on the first and the second DBH measurement as the compound annual growth rate of the trees basal area

 Stand data
_All stand variables were calculated for the second inventory._

mDBH: Mean diameter at breast height (mm)

iqrDBH: Interquartile range of diameter at breast height (mm)

BA: Basal area per hectare (m2 ha-1)

N: Number of trees per hectare (ha-1)

 Climate data
_Both climate variables were calculated for the period between the second and the third inventory._

P: Mean annual precipitation sum (mm)

mT: Mean annual air temperature (°C)

en: Calibration data

format: CSV

media_type: text/csv

empirical-mortality-models

display_name: empirical-mortality-models

forest-reserves

display_name: forest-reserves

inventory-data

display_name: inventory-data

tree-growth

display_name: tree-growth

tree-mortality

display_name: tree-mortality


en:
Attention: this data is not updated after 2022 anymore.
This dataset contains the statistics on the number of avalanche fatalities per **calendar year** in Switzerland. The data collection commences with the beginning of the year 1937. After the completion of a hydrological year, which is the standard way avalanche fatalities are summarized in Switzerland and ends on the 30th of September, the new data is appended to the existing dataset.
If you require annual statistics per hydrological year, please download the data from here: [https://www.envidat.ch/dataset/avalanche-fatalities-switzerland-1936]
The following information is contained (by column and column title):
 - year
 - number of fatalities in the backcountry (=tour)
 - number of fatalities in terrain close to ski areas (=offpiste, away from open and secured ski runs)
 - number of fatalities on transportation corridors including ski runs, roads, railway lines (=transportation.corridors)
 - number of fatalities in or around buildings or in settlements (= buildings)
 - sum (of all four categories)
The definitions for these four categories, as described in the guidelines to the avalanche accident database are:
tour:
activities include back-country ski, snowboard or snow-shoe touring
offpiste:
access from ski area, generally from the top of a skilift with short hiking distances
transportation.corridors (Techel et al., 2016):
people travelling or recreating on open or temporarily closed transportation corridors (e.g. a road user or a skier on a ski run) and people working on open or closed transportation corridors (e.g. maintenance crews on roads, professional rescue teams)
buildings (Techel et al., 2016):
people inside or just outside buildings, and workers on high alpine building sites

en: Number of avalanche fatalities per calendar year in Switzerland since 1937

avalanche-accident-statistics

display_name: avalanche-accident-statistics

avalanche-fatalities

display_name: avalanche-fatalities

fatalities-in-or-around-buildings

display_name: fatalities-in-or-around-buildings

fatalities-in-settlements

display_name: fatalities-in-settlements

fatalities-in-the-backcountry

display_name: fatalities-in-the-backcountry

fatalities-on-transportation-corridors

display_name: fatalities-on-transportation-corridors


en:
Attention: this data is not updated after 2022 anymore.
This data collection contains information concerning all accidents by snow avalanches causing at least one fatality in Switzerland. The data set commences on 01/10/1995. After the completion of a hydrological year, the new data is added.
The following information is provided:
 * avalanche identifier
 * date of the accident
 * accuracy of the date in range of days before and after
 * canton
 * name of the locality
 * start zone of the avalanche
  * coordinates (Swiss coordinate system, approximately in middle of start zone)
  * accuracy of the coordinates in meters
 * elevation (in meteres above sea level, app. in middle of start zone)
 * slope aspect (main orientation of start zone)
 * slope inclination (in degree, steepest point within start zone)
 * number of dead persons
 * number of caught persons
 * number of fully buried persons
 * forecasted avalanche danger level
 * activity/location of the accident party at the time of the incident

en: avalanche-accident-statistics avalanche-accidents avalanche-fatalities number-of-caught-persons number-of-dead-persons

en: Fatal avalanche accidents in Switzerland since 1995-1996

avalanche-accidents

display_name: avalanche-accidents

number-of-caught-persons

display_name: number-of-caught-persons

number-of-dead-persons

display_name: number-of-dead-persons


en:
 Dataset of an experimental campaign of induced rockfall in Tschamut, Grisons, Switzerland.

The data archive contains site specific geographical data such as DEM and orthophoto as well as the deposition points of manually induced rockfall by releasing differently shaped boulders with 30–80 kg of mass. Additionally available are all the StoneNode data streams for rocks equipped with a sensor. The data set consists of

* Deposition points from two series (wet (27/10/2016) and frozen (08/12/2016) ground)
* Digital Elevation Model (grid resolution 2 m) obtained via UAV
* Orthophoto (5 cm resolution) obtained via UAV
* Digitized rock point clouds (.pts input files for RAMMS::ROCKFALL)
* StoneNode v1.0 raw data stream for equipped rocks.

Further information is found in

* A. Caviezel et al., _Design and Evaluation of a Low-Power Sensor Device for Induced Rockfall Experiments_, IEEE Transactions on Instrumentation and Measurement, 2018, 67, 767-779, http://ieeexplore.ieee.org/document/8122020/
* P. Niklaus et al., _StoneNode: A low-power sensor device for induced rockfall experiments_, 2017 IEEE Sensors Applications Symposium (SAS), 2017, 1-6, http://ieeexplore.ieee.org/document/7894081/

en: dem deposition-points induced-rockfall natural-hazards rockfall rockfall-experiments rockfall-runout sensor-stream stonenode stonenodedata

envidat

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

en: EnviDat: the Environmental Data Portal

en: Induced Rockfall Dataset (Small Rock Experimental Campaign), Tschamut, Grisons, Switzerland

en:
 Induced Rockfall Experimental Data, Tschamut, GR, Switzerland

The archive contains site specific geographical data as well as the deposition points of manually induced rockfall by releasing differently shaped boulders with 30–80 kg of mass. Additionally availabe are the StoneNode v1.0 sensor streams for the equipped rocks.

The _OverviewFigures_ file serves as quick representation of the included data. It also contains the overview table for the rock masses in order to set the dimensions accordingly in RAMMS::ROCKFALL.

The archive contains the following folders:
<\ul>
* DEM: ArcGIS compatible DEM Tschamut_DEM_2m (grid resolution of 2 m) as well as the .asc grid used in RAMMS::ROCKFALL simulations
* _DepositionPoints_: containing two folders _RF Tschamut Frozen_ and _RF Tschamut WET_ containing each a shapefile with the complete deposition data of each series as well as deposition shapfiles for each rock shape.
* _DigitizedRocks_: Digitized point clouds of the used rocks as used for RAMMS::ROCKFALL simulations (.pts files) (dimensions have to be checked).
* _Orthofoto_: Orthophoto of the experimental site obtained via UAV with 5 cm resolution.

en: Induced Rockfall Data, Tschamut, GR

en: Corresponding StoneNode v1.0 data streams belonging to the deposition points.

en: StoneNode v1.0 Data for equipped experimental Runs.

dem

display_name: dem

deposition-points

display_name: deposition-points

induced-rockfall

display_name: induced-rockfall

natural-hazards

display_name: natural-hazards

rockfall

display_name: rockfall

rockfall-experiments

display_name: rockfall-experiments

rockfall-runout

display_name: rockfall-runout

sensor-stream

display_name: sensor-stream

stonenode

display_name: stonenode

stonenodedata

display_name: stonenodedata


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

en: Ecosystem coupling and multifunctionality - exclosure experiment

educ

en: Education, culture and sport

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: Datafile

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

subalpine

display_name: subalpine

swiss-national-park

display_name: swiss-national-park

vertebrates

display_name: vertebrates


en:
Book of abstracts from the virtual conference "From Plans to Land Change: Dynamics of Urban Regions"

Cities and urban regions are among the most dynamic land-use systems in the world, with dramatic consequences for the provision of ecosystem services and the livelihood of people. Planning is a multifaceted activity with extensive experience in the management of these urbanization processes. However, our understanding of planning’s contribution to shaping urban land use, form and structure is still incomplete, with serious consequences for the efficacy of urban planning and land change models.

This international conference aims to bring together the community of scholars working on planning evaluation and urban modelling. The participants are offered the opportunity to present their current research and to discuss how theoretical developments, data sources, comparative studies and modelling approaches might advance the field.

The conference was financially supported by the CONCUR project and sustained by Swiss Federal Research Institute WSL.

en: concur land-change landscape-planning urban-landscape urban-planning

en: From Plans to Land Change: Dynamics of Urban Regions. Book of Abstracts

concur

display_name: concur

land-change

display_name: land-change

landscape-planning

display_name: landscape-planning

urban-landscape

display_name: urban-landscape

urban-planning

display_name: urban-planning


en:
Raw data supporting the paper "Countrywide wild bee taxonomic and functional diversity reveal a spatial mismatch between alpha and beta-diversity facets across multiple ecological gradients". It contains taxonomic and functional metrics in 3343 community-plots distributed across Switzerland. The calculated metrics are:
- Alpha taxonomic community metrics: species richness and Shannon diversity
- Alpha functional community metrics: Functional richness (using the Trait Onion Peeling index, TOP), functional eveness (using the Trait Even Distribution index, TED) and the functional dispersion.
- Community weighted means of 8 functional traits
- The local community contributions on the functional and taxonomic beta diversity (LCBD).

The dataset also includes the following:
- The used predictors to model the spatial distribution of the community metrics (climate PCA, vegetation PCA, land-use metrics, beekeeping intensity).
-The three types of protected areas, defined according to the protective measures.
- The model evaluation, variable importance and partial dependece data.

en: anthophila beta-diversity biodiversity climate community-indices elevation-gradient functional-diversity hymenoptera predictive-modelling protected-areas resource-availability switzerland urbanization wild-bee

en: Data on wild bee taxonomic and functional diversity in Switzerland

en:
Response data used for the modeling.
Lat: latitude community plot
Lon: longitude community plot
Richness: species richness
Shannon: Shannon diversity index
FDis: functional dispersion
TOP: Trait Onion Peeling (functional richness)
TED: Trait Even Distribution (functional evenness)
LCBD_taxo: local community contributions to taxonomic beta diversity
LCBD_fun: local community contributions to functional beta diversity
ITD: community weighted means inter-tegula distance
feeding_specialization: community weighted means feeding specialization
tong_length: community weighted means tongue length
phenostart: community weighted means start of the phenology
phenoduration: community weighted means duration of the phenoloy
cleptoparasite: community weighted means cleptoparasites
belowgound: community weighted means proportion belowground
solitary: community weighted means proportion solitary

en: Taxonomic and functional metrics in the community plots

en: Protected areas considered, divided in three groups and rasters: protected areas sensu stricto, protected areas sensu lato and all protected areas

en: Protected areas

en: The compress file containes a set of txt files with the variable importance, the model evaluation metrics and the partial dependence plots of each of the responses used (alpha and beta taxonomic and functional diversity metrics; community weighted means of 8 functional traits)

en: Variable importance, model evaluation, partial dependence plots

en:
The .zip file contains the rasters of the environmental predictors and the predicted responses:
-  **Environmental predictors.**:
  -  The raster on the climate contains the PCA axes on the CHELSA variables.
  -  The raster on resource availability contains the PCA axes on plant communities
  -  The raster on land-use contains the land-use composition at 2500 m.
  -  The raster on beekeeping intensity contains thedensity of hives within 2500 m
-  **Responses**:
- The predicted responses (alpha and beta taxonomic and functional metrics and the traits) without masking the waterbodies, used in the analyses (Diversity_stack_revised_Selected_descriptors.tif). It contains a stack of 20 responses in this order: "belowgound", "cleptoparasite","FDis", "feeding_specialization", "FEve", "FRic", "InvSimpson", "ITD","LCBD_fun" ,"LCBD_taxo","phenoduration", "phenostart", "Rao", "Richness", "Shannon", "Simpson","solitary", "TED", "tong_length", "TOP". "FEve", "FRic", "InvSimpson","Rao", "Simpson" were not included in the linked paper.
- The predicted responses (alpha and beta taxonomic and functional metrics and the traits) masking the waterbodies (masked.stack.all.diversity.tiff). It includes a stack of 15 responses (excludes "FEve", "FRic", "InvSimpson","Rao", "Simpson").

en: Spatial environmental predictors and responses

en: Zip file containing two rasters: the digital elevation model of Switzerland and the waterbodies of Switzerland.

en: Elevation and waterbodies

en: Text file containing the scores of the 8 used traits. The data originates from the European trait database (compiler: Stuart Roberts; pollinator loss module of the EU- FP6 ALARM project).

en: Wild bee trait data

anthophila

display_name: anthophila

beta-diversity

display_name: beta-diversity

biodiversity

display_name: biodiversity

climate

display_name: climate

community-indices

display_name: community-indices

elevation-gradient

display_name: elevation-gradient

functional-diversity

display_name: functional-diversity

hymenoptera

display_name: hymenoptera

predictive-modelling

display_name: predictive-modelling

protected-areas

display_name: protected-areas

resource-availability

display_name: resource-availability

switzerland

display_name: switzerland

urbanization

display_name: urbanization

wild-bee

display_name: wild-bee


en:
The European Snow Booklet (ESB) is a book of reference for snow measurements that has been produced through collaboration with many European snow practitioners and snow scientists in the framework of the European Cooperation in Science and Technology (COST) Action ES1404 “A European network for a harmonised monitoring of snow for the benefit of climate change scenarios, hydrology and numerical weather prediction (HarmoSnow)”. The ESB provides a unique collection of information about operational snow observations in the European countries and the methods used to perform basic measurements of snow on the ground: snow depth (HS), depth of snowfall (HN), water equivalent of the snow cover (SWE) and presence of snow on the ground (PSG). Information and station metadata (for example location, elevation) for these basic snow variables were collected through a comprehensive survey, the ESB questionnaire between August 2017 and March 2018. Numerous institutions of 38 European countries provided detailed information describing the status of the operational snow observations and the methods used at the time of the survey. Based on the information provided, a country report was written for each European country. Similarities and differences among the countries, that is, the choice of snow variables to be measured, the measurement principles applied, the number of stations, or the spatial and elevational station distribution are pointed out. Thus the collection of country reports demonstrates the relevance of snow measurements for each country. Thus, the intention of the ESB is to foster better knowledge transfer regarding snow measurements between the snow science and operational communities and to improve the communication of information to the general public.

For detailed information on the European countries, we refer to the ESB, which can be downloaded here (envidat.ch). Please note that the ESB is not a living document and information and station metadata are from August 2017 till March 2018, except for Latvia (metadata updated in December 2018).

envidat

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

en: EnviDat: the Environmental Data Portal

en: European Snow Booklet – an Inventory of Snow Measurements in Europe

educ

en: Education, culture and sport

en:
The core of the European Snow Booklet (ESB), the country reports of 38 European countries, are based on information and metadata on snow measurements collected through a comprehensive survey, the ESB Questionnaire, between August 2017 and March 2018. The station metadata (for example location, elevation, measurement start date) from each country was provided by one or several institutions responsible for snow observations. By answering the questionnaire the contacts agreed that the information and metadata provided could be presented in the ESB. For cases where institutions indicated that information on station locations could be made publicly available, the metadata for the variables snow depth (HS), depth of snowfall (HN) and water equivalent of the snow cover (SWE), is additionally provided here for download (METADATA.xlsx).
Please note that not all institutions gave permission to publish their station metadata. This metadata has to be requested from the non-personal institution contacts provided in the METADATA.xlsx file. In some cases, however, no institutional contact is available and thus the contact of the country representative who filled in the questionnaire is used.
For current, updated station metadata we refer to the (non-personal) institutional contacts provided in METADATA.xlsx and/or the institution webpages. Note, however, that we cannot guarantee for completeness of the dataset for all countries because operational networks are prone to changes.

en: European Snow Booklet public metadata

en:
Here you can find the list of all lead authors of the different chapters of the European Snow Booklet (ESB).
In addition a list of the editorial board that reviewed the ESB is given.

en: List of authors and list of the editorial board of the European Snow Booklet

en: Please find here the web version of the COST European Snow Booklet (ESB).

en: COST European Snow Booklet (ESB)

en: DORA Link of the COST European Snow Booklet (ESB).

en: COST European Snow Booklet (ESB) - DORA Link

format: HTML

media_type: text/html

depth-of-snowfall

display_name: depth-of-snowfall

harmonisation-of-snow-measurements

display_name: harmonisation-of-snow-measurements

snow-depth

display_name: snow-depth

snow-measurement-methods

display_name: snow-measurement-methods

water-equivalent-of-the-snow-cover

display_name: water-equivalent-of-the-snow-cover


en: The following two tables contain information about the data sources of the values reported in Table 1 and 2 in the paper “Plant and root-zone water isotopes are difficult to measure, explain, and predict: some practical recommendations for determining plant water sources” published in the journal 'Methods in Ecology and Evolution'.

en: ecohydrology endmember-mixing-models plant-water-uptake review root-zone stable-water-isotopes uncertainties

en: Data set of: Plant and root-zone water isotopes are difficult to measure, explain, and predict: some practical recommendations for determining plant water sources

en: The following two tables contain information about the data sources of the values reported in Table 1 and 2 in the paper “Plant and root-zone water isotopes are difficult to measure, explain, and predict: some practical recommendations for determining plant water sources” published in the journal ‘Methods in Ecology and Evolution’.

en: Data set of MEE-20-04-264

ecohydrology

display_name: ecohydrology

endmember-mixing-models

display_name: endmember-mixing-models

plant-water-uptake

display_name: plant-water-uptake

review

display_name: review

root-zone

display_name: root-zone

stable-water-isotopes

display_name: stable-water-isotopes

uncertainties

display_name: uncertainties


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

en: edna fish-composition marine marseille mediterraneaen teleo

envidat

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

en: Environmental DNA Marine France Calanques 2022

en: Please use cyberduck to download for the moment

en: Data access

edna

display_name: edna

fish-composition

display_name: fish-composition

marine

display_name: marine

marseille

display_name: marseille

mediterraneaen

display_name: mediterraneaen

teleo

display_name: teleo


en: The dataset contains hydrochemical data collected from spring to fall 2022 in the Haute-Mentue catchment, Switzerland. This hydrochemical data includes solute concentrations and stable isotopes of oxygen and hydrogen in water molecules, measured in streamwater, soil water, groundwater, and rainfall samples. Samples were collected during eight rainfall events with higher temporal resolution (hourly) as well as at lower resolution between events. A detailed description of the dataset is provided in the documentation.

en: catchment catchment-data groundwater hydrogen-isotopes oxygen-isotopes solutes stream-water

envidat

en: EnviDat: the Environmental Data Portal

en: Hydrochemical Data Collected during Spring-Fall 2022 in the Haute-Mentue Catchment

educ

en: Education, culture and sport

en: This document provides a detailed description of the hydrochemical dataset, including, among other things, an overview of the dataset content, an explanation of the column headers, a description of the locations where samples were collected, and an explanation of the abbreviations used in the dataset.

en: This dataset includes mean concentrations of solutes (Calcium, Iron, Magnesium, Sodium, Potassium, Boron, Nitrate, Sulfate, and Chloride) and stable isotope values (hydrogen and oxygen) in water molecules. These were measured in precipitation, groundwater, soil water, and surface water samples collected from the Haute-Mentue catchment in Switzerland during Spring and Fall 2022. Detailed information is available in the accompanying documentation (documentation_for_the_hydrochemical_data_collected_during_spring_fall_2022_in_the_haute-mentue_catchment.pdf).

catchment

display_name: catchment

catchment-data

display_name: catchment-data

groundwater

display_name: groundwater

hydrogen-isotopes

display_name: hydrogen-isotopes

oxygen-isotopes

display_name: oxygen-isotopes

solutes

display_name: solutes

stream-water

display_name: stream-water


en: The dataset contains hydrochemical data collected from spring to fall 2021 in the Erlenbach catchment, Switzerland. This hydrochemical data includes solute concentrations and stable isotopes of oxygen and hydrogen in water molecules, measured in streamwater, soil water, groundwater, and rainfall samples. Samples were collected during seven rainfall events with higher temporal resolution (hourly) as well as at lower resolution between events. A detailed description of the dataset is provided in the documentation.

en: catchment catchment-data erlenbach groundwater hydrogen-isotopes oxygen-isotopes precipitation solutes stream-water

en: Hydrochemical Data Collected during Spring-Fall 2021 in the Erlenbach Catchment

en: This dataset includes mean concentrations of solutes (Calcium, Iron, Magnesium, Sodium, Potassium, Silicon, Nitrate, Sulfate, and Chloride) and stable isotope values (hydrogen and oxygen) in water molecules. These were measured in precipitation, groundwater, soil water, and surface water samples collected from the Erlenbach catchment and its close vicinity in Switzerland during Spring and Fall 2021. Detailed information is available in the accompanying documentation (documentation_for_the_hydrochemical_data_collected_during_spring_and_fall_2021_in_the_erlenbach_catchment.pdf).

erlenbach

display_name: erlenbach

precipitation

display_name: precipitation


en:
This dataset was used to analyse effects of different biodiversity and functional group treatments, fertilizer and fungicide applications as well as weeding of vascular plants on the species richness and species composition of bryophytes for the following publication: Lin M., Bergamini A., Pichon N.A., Allan E, Boch S. 2025. Nitrogen enrichment and vascular plant richness loss reduce bryophyte richness. Scientific Reports.
In this study we surveyed 96 of 216 2 m x 2 m experimental plots of the PaNDiv experiment, a large grassland field experiment in the Swiss lowlands (Pichon et al. 2020). In the PaNDiv experiment four experimental treatments were applied in a full-factorial design manipulating: (1) the nitrogen availability (through fertilization), (2) the presence of fungal pathogens (through fungicide application), (3) the functional composition of the vascular plant community (represented here by community-weighted mean (CWM) SLA), and (4) the vascular plant richness (sowing of either 1, 4, 8 or 20 species). To maintain the original sown vascular plant species richness and composition, one part of each plot (1.5 m × 2 m) was weeded, while the other part has been left unweeded since the beginning of the experiment (0.5 m × 2 m).
On each plot we surveyed two subplots, the unweeded subplot and a weeded subplot of the same area (0.5 m × 2 m). On each subplot we established a complete list of all bryophyte species together with an estimate of their cover.
The provided excel file contains three sheets:
1.	A sheet with raw species lists of all plots surveyed together with information on all treatments and an estimation of the percentage cover of vascular plants in a summer campaign in August 2022. Cover of bryophytes was estimated for each species in percent.
2.	A sheet with a list of all bryophyte species with its growth form (acroarpous/pleurocarpous)
3.	A sheet with some explantations
By means of the provided R code and the data in the excel file, all analyses can be repeated.
More details to the data sampled can be found in Lin et al (2025).

en: biodiversity-experiment biomass bryophytes functional-traits fungicide grassland moss nitrogen pandiv species-richness

en: Data on bryophyte diversity and treatment factors in the PaNDiv experiment

en: main data as used in Lin et al. 2025

biodiversity-experiment

display_name: biodiversity-experiment

biomass

display_name: biomass

bryophytes

display_name: bryophytes

functional-traits

display_name: functional-traits

fungicide

display_name: fungicide

grassland

display_name: grassland

moss

display_name: moss

nitrogen

display_name: nitrogen

pandiv

display_name: pandiv

species-richness

display_name: species-richness


en:
This dataset includes geomorphic predictors and plant biodiversity patterns in the Hengduan Mountains, published in the Geological Society of London special volume: Asian Geodynamics, Climate and Biodiversity (https://doi.org/10.1144/SP549-2024-17).
The geomorphic predictors include catchment-restricted relief and chi maps, while the climate predictors comprise site water balance, growing degree days, and climate change velocity from the Last Glacial Maximum (LGM) to the present.
The plant biodiversity patterns are represented by a plant richness map for 13,321 species in the Hengduan Mountains. Species-level plant range maps are available in the dataset, previously published under DOI: 10.16904/envidat.424.

en: climate-history endemism plant-biodiversity relief tectonic-faults

envidat

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

en: Tectonic and climatic controls on plant biodiversity in the Hengduan Mountains China

climate-history

display_name: climate-history

endemism

display_name: endemism

plant-biodiversity

display_name: plant-biodiversity

relief

display_name: relief

tectonic-faults

display_name: tectonic-faults


figures-perspective-urban-beekeeping

en:
Data and code from the perspective paper "When honeybees comes to town"
The .r file provides the code to generate the figures.
In addition, this repository contains the data for the figures 1-3.
For Figure 4, part of the data is confidential, Please, refer to the contacts provided:
- For the distribution of hives in Zurich (2018): https://www.zh.ch/de/gesundheitsdirektion/veterinaeramt.html
- For the overheating map of Zurich: Prof. Dr. Eberhard Parlow / Stadt Zurich (https://www.zh.ch/de/umwelt-tiere/umweltschutz/umweltpraxis/definitionsseite/2012/68/zup068_2012_a0030_klimaanalyse-pdf.html)

en: diversity-distributions hymenoptera insects urban-beekeeping urban-ecology wildbees

envidat

en: EnviDat: the Environmental Data Portal

en: Figures perspective urban beekeeping

title_for_slug: figures-perspective-urban-beekeeping

en:
 The file shows the results from the literature review. Briefly, we searched papers using google scholar search engine using the following query: (“WILD BEE OR WILDBEE”)(“URBAN” OR “CITY”), and limited the time span from 2010-2023. The search query returned 200 candidate papers. In addition, we complemented the candidate papers from the literature research performed by Ferrari & Polidori (2022), adding 22 additional candidate papers. To select papers, we checked that (1) were conducted in urban areas; (2) sampled the whole bee community; (3) provided data on abundance of wildbees; (4) provided data on honeybees; and (5) provided individual abundance data of each wild bee species.
The dataset contains the following:
-Article_ID: ID for the specific article in the form "A1", "A2"..."An"
- Title: of the article
- Year: of publication
- Journal: of publication
- Publisher:
- Link: link to the publication
- DOI: when applicable
- Total abundance wild bees reported: was the total number of collected bees reported? Logical (Y/N)
- Honey bee abundance reported: was thenumber of honeybees collected reported? 	Logical (Y/N)
- Abundance per wild bee species: was the number of wildbee species sampled provided? Logical (Y/N)
- Select proportion: paper selected to calculate the proportion of honeybees and wildbees.
- Select RAD: paper selected to compute the rank-abundance distribution diagram
Comment: comments on the papers, data availability, etc.

en: Results literature review

en: DEPRECATED. Data growth urban beekeeping

en: Coordinates (LatLon format) of the cities where data from urban bee ecology studies was used.

en: Coordinates studied cities

en: Outdated, use the new resource "Propotion urban honeybees and wildbees"

en: Proportion honeybees and wildbees

en: Outdated, use the new resource

en: Data rank-abundance distribution urban bees

en: The dataset contains the number of beehives per registered beekeeper ID (annonymised) in four Swiss cities (Bern, Lausanne, Geneve, Zurich).

en: DEPRECATED. Distirbution beehives among beekeepers

en:
The dataset contains the average NDVI values around beehives in Zurich at three spatial scales (250, 500 and 1000 m). It contains 3 columns_
- buffer: indicating the spatial scale
- ID: hive ID (annonymised)
- mean.NDVI: mean NDVI value

en: NDVI values within 3 buffers  in hives in Zurich

en:
The dataset contains the average overheating values around beehives in Zurich at three spatial scales (250, 500 and 1000 m). It contains 4 columns:
- buffer: indicating the spatial scale
-ID: hive ID (annonymised)
- mean.overwarming: mean overheating value, expressed in degrees Kelvin
-mena.overwarming.cor = transformed values do degrees Celsius

en: Local overheating values within 3 buffers in hives in Zurich

en: Deprecated version of the R script

en: R script for the figures V1

format: OCTET

en: R script for the figures

en: R script for the figures V2

en: The dataset contains the number of beehives per registered beekeeper ID (annonymised) in four Swiss cities (Bern, Lausanne, Geneve, Zurich) and Paris.

en: Distribution beehives among beekeepers

en:
The dataset contains the data of the growth of urban beekeeping in different cities.
For each city in a given year, it contains the following:
Continent.
Country.
City: the name of the city
Year: the year when the information was collected
Area: of the city
Total N. beekeepers: when available, the estimated number of beekeepers in that city for that given year
Total N. hives: when available, the estimated number of beehives in that city for that given year
Density: the total number of hives divided by the city area
Reference: the source of the information.

en: Data growth urban beekeeping

en:
The dataset contains the proportion of wildbees and honeybees in the different studies obtained from the literature review.
Article_ID: ID for each article
DOI
Authors
Year: publication year
Duration sampling (years): numerical
Start_sampling: numerical, date
End_sampling: numerical, date
Continent
Country
N. cities: number of cities sampled in the article. Numerical.
City
Sampling type: categorical. Levels: active (e.g., Hand-netting); passive (e.g., pantraps. trap-nests); both (combination of passive and active methods).
Sampling methodology: categorical. Levels: direct observations, hand-netting, pantraps, interception traps, vane traps.
Number sites: total number of study sites.
Abundance honeybees: number of honeybees recorded
Abundance wild bees: number of wildbees recorded
Total bees: total number of bees recorded.
Proportion honeybees: Abundance of honeybees / Total number of bees
Proportion wildbees: Abundance of wildbees / Total number of bees

en: Proportion urban honeybees and wildbees

en:
Abundance data at the species level per used dataset for the rank abundance distribution (RAD).
40 datasets used.

en: Species-abundance data

diversity-distributions

display_name: diversity-distributions

hymenoptera

display_name: hymenoptera


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/)

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

envidat

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

en: EnviDat: the Environmental Data Portal

en: Automated detection of invasive alien plants along highways

educ

en: Education, culture and sport

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 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 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.

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