en: example-applications forest-dynamics forest land-use treemig r-package climate-change bioclimatic-variables spatial-modelling species-migration forest-management

en: R-script to install the TreeMig framework and start the graphical user interface

en: Where the environmental and land use input data come from and how they were processed

en:
1) Simulation environment TMEnvironmentExampleApplications for the simulation of the case study applications. It contains a) simulation settings (folder C), b) species parameters (folder P), c) folders S, R and P for the state files and results and plots to be produced, and the binaries of the TreeMig model.
2) Input data for Switzerland in TMInputData (Climate, soil, land cover, DEM)
3) Several R scripts (folder Scripts) to run and plot the simulations directly from R without having to use the graphical user interface.
For learning how to use TreeMig we recommend the starter kit https://www.doi.org/10.16904/envidat.533.

en:
The [TreeMig framework](https://treemig.wsl.ch/en/) allows for an easy application of the forest landscape model TreeMig for simulating forest dynamics in space under changing environmental and land use conditions.
Here, case study examples in Switzerland are given that simulate the dynamics and spatial spread of competing tree species in a region in Switzerland, the invasion of a hypothetical invasive tree species, and the control of this species via a management model coupled to TreeMig. The datasets consist of the installation- and GUI starting-script, example environmental input data for Switzerland, the simulation environment, and further R-scripts for running the simulations and plotting the simulation results directly from R and for coupling TreeMig to the forest management model.

bioclimatic-variables

display_name: bioclimatic-variables

climate-change

display_name: climate-change

example-applications

display_name: example-applications

forest

display_name: forest

forest-dynamics

display_name: forest-dynamics

forest-management

display_name: forest-management

land-use

display_name: land-use

r-package

display_name: r-package

spatial-modelling

display_name: spatial-modelling

species-migration

display_name: species-migration

treemig

display_name: treemig

en: Case study applications demonstrating the use and potential of the TreeMig framework v1


maintainer: Franziska Gerber

en: aws python cryowrf consistent antarctica

state: active

type: dataset

en: Scripts to preprocess (and download for some databases) atmospheric weather station data. Furthermore, a list of stations and a map can be created to have an overview.

format: SERVICE

en:
There are many sources providing atmospheric weather station data for the Antarctic continent. However, variable naming, timestamps and data types are highly variable between the different sources. The published python code intends to make processing of different AWS sources from Antarctica easier. For all datasets that are taken into account variables are renamed in a consistent way. Data from different sources can then be handled in one consistent python dictionary.

The following data sources are taken into account:

* AAD: Australian Antarctic Division (https://data.aad.gov.au/aws)
* ACECRC: Antarctic Climate and Ecosystems Cooperative Research Centre by the Australian Antarctic Division
* AMRC: Antarctic Meteorological Research Center (ftp://amrc.ssec.wisc.edu/pub/aws/q1h/)
* BAS: British Antarctic Survey (ftp://ftp.bas.ac.uk/src/ANTARCTIC_METEOROLOGICAL_DATA/AWS/; https://legacy.bas.ac.uk/met/READER/ANTARCTIC_METEOROLOGICAL_DATA/)
* CLIMANTARTIDE: Antarctic Meteo-Climatological Observatory by the italian National Programme of Antarctic Research (https://www.climantartide.it/dataaccess/index.php?lang=en)
* IMAU: Institute for Marine and Atmospheric research Utrecht (Lazzara et al., 2012), https://www.projects.science.uu.nl/iceclimate/aws/antarctica.ph
* JMA: Japan Meteorological Agency (https://www.data.jma.go.jp/antarctic/datareport/index-e.html)
* NOAA: National Oceanic and Atmospheric Administration (https://gml.noaa.gov/aftp/data/meteorology/in-situ/spo/)
* Other/AWS_PE: Princess Elisabeth (PE), KU Leuven, Prof. N. van Lipzig, personal communication
* Other/DDU_transect: Stations D-17 and D-47 (in transect between Dumont d’Urville and Dome C, Amory, 2020)
* PANGAEA: World Data Center (e.g. König-Langlo, 2012)

Important notes

* Information about data sources is available. Some downloading scripts are included in the provided code. However, users should make sure to comply with the data providers terms and conditions.
* Given changing download options of the differnent institutions the above links may not permanently work and data has to be retrieved by the user of this dataset.
* No quality control is applied in the provided preprocessing software - quality control is up to the user of the datasets. Some dataset are quality controlled by the owner.

Acknowledgements
--------------------------
We thank all the data providers for making the data publicly available or providing them upon request. Full acknowledgements can be found in Gerber et al., submitted.

References
---------------
Amory, C. (2020). “Drifting-snow statistics from multiple-year autonomous measurements in Adélie Land, East
Antarctica”. The Cryosphere, 1713–1725. doi: 10.5194/tc-14-1713-2020

Gerber, F., Sharma, V. and Lehning, M.: CRYOWRF - a validation and the effect of blowing snow on the Antarctic SMB, JGR - Atmospheres, submitted.

König-Langlo, G. (2012). “Continuous meteorological observations at Neumayer station (2011-01)”. Alfred Wegener
Institute, Helmholtz Centre for Polar and Marine Research, Bremerhaven, PANGAEA, doi: 10.1594/PANGAEA.
775173

antarctica

display_name: antarctica

aws

display_name: aws

consistent

display_name: consistent

cryowrf

display_name: cryowrf

python

display_name: python

educ

fr: Éducation, culture et sport

de: Bildung, Kultur und Sport

en: Education, culture and sport

it: Istruzione, cultura e sport

envidat

fr: EnviDat: le portail de données environnementales

de: EnviDat: das Umwelt-Datenportal

en: EnviDat: the Environmental Data Portal

it: EnviDat: il portale dei dati ambientali

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

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

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

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

political_level: other

wsl

capacity: public

type: organization

approval_status: approved

key: guid

key: uri

value: Envidat Harvester

en: Preprocessing Antarctic Weather Station (AWS) data in python


maintainer: Robert Pazúr

en: machine-learning vegetation-indices switzerland cropland grassland remote-sensing phenology sentinel-2 habitat agriculture

en: Mask of unsealed surfaces of Switzerland based on 3 years Sentinel-2 NDVI 95th percentile threshold value: 0.7 (v1.0)

media_type: image/tiff

en: !!! Please check out the newer version in this repository !!! Assuming that sealed surfaces have little or no phenological response we calculated a mask of unsealed surfaces based on the 3 years (2017-2019) Sentinel-2 NDVI 95th percentile threshold value: 0.7.

format: TIFF

en: (current version) Mask of unsealed surfaces of Switzerland based on 3 years Sentinel-2 NDVI 95th percentile threshold value: 0.6 (v1.5)

en: Assuming that sealed surfaces have little or no phenological response we calculated a mask of unsealed surfaces based on the 3 years (2017-2019) Sentinel-2 NDVI 95th percentile threshold value: 0.6.

format: GeoTIFF

en: (current version) Cropland, grassland, and shrubland map of Switzerland (v.1.5)

en: Cropland, grassland, and shrubland map of Switzerland (v1.0)

en: !!! Please check out the newer version in this repository !!! (1) cropland; (2) grassland; (3) shrubland; other LC classes are masked out from the map

en: Cropland and grassland map of Switzerland  (v.1.0)

en: !!! Please check out the newer version in this repository !!! (1) cropland; (2) grassland; other LC classes are masked out from the map

en: (current version) Mask of unsealed surfaces of Switzerland based on 3 years Sentinel-2 NDVI 95th percentile threshold value: 0.7 (v1.5)

en: GEE (Google Earth Engine) script (JavaScript) to derived the output map  (v1.0)

en: !!! Please check out the newer version in the repository !!! The code used in Google Earth Engine to derive the cropland, grassland and shrubland map of Switzerland

en: Mask of unsealed surfaces of Switzerland based on 3 years Sentinel-2 NDVI 95th percentile threshold value: 0.6  (v1.0)

en:
!!! Please check out the newer version in the repository !!!
Mask of unsealed surfaces of Switzerland based on 3 years (2017-2019) Sentinel-2 NDVI 95th percentile threshold value: 0.6

en: (current version) Cropland and grassland map of Switzerland (v.1.5)

en: GEE (Google Earth Engine) script (JavaScript) to derived the output map  (v1.5)

en: The code used in Google Earth Engine to derive the cropland, grassland and shrubland map of Switzerland. Compare to the previous version the newer version includes the shadow masking procedure which might be important in the mountainous areas.

en: We developed a map of cropland and grassland allocation for Switzerland based on several indices dominantly derived from Sentinel-2 satellite imagery captured over multiple growing seasons. The classification model was trained based on parcel-based data derived from landholder reporting. The mapping was conducted on Google Earth Engine platform using random forest classifier. Areas of high vegetation, shrubland, sealed surface and non-vegetated areas were masked out from the country-wide map. The resulting map has high accuracy in lowlands as well as mountainous areas.

agriculture

display_name: agriculture

cropland

display_name: cropland

grassland

display_name: grassland

habitat

display_name: habitat

machine-learning

display_name: machine-learning

phenology

display_name: phenology

remote-sensing

display_name: remote-sensing

switzerland

display_name: switzerland

vegetation-indices

display_name: vegetation-indices

en: Cropland and grassland map of Switzerland based on Sentinel-2 data


maintainer: Elisabeth Hafner

en: satellite avalanche avalanche-hazard-mapping validation snow

en: Satellite Avalanche Mapping Validation data and data description

media_type: application/zip

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

format: ZIP

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

Coordinate system: CH1903+_LV95

The generation of this dataset is described in detail in:

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

avalanche

display_name: avalanche

avalanche-hazard-mapping

display_name: avalanche-hazard-mapping

satellite

display_name: satellite

snow

display_name: snow

validation

display_name: validation

educ

en: Education, culture and sport

envidat

en: EnviDat: the Environmental Data Portal

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

en: Satellite avalanche mapping validation data


en: microbial-respiration soil-respiration microbial-biodiversity ecosystem-functions beta-diversity

en: Bacterial amplicon sequencing

en: Bacterial ASVs and taxonomic tables

format: XLS

en: Fungal amplicon sequencing

en: Fungal ASVs and taxonomic tables

en: Microbial functions and metadata

en: Extracellular enzyme activities, respiration and sites metadata

en: Structural and functional changes of microbial communities in ephemeral stream sediments and adjacent soils between was assessed in an artificial newly created catchment at 3 and 13 years after catchment construction. Bacterial and fungal communities, respiration and extracellular enzyme activities were assessed.

beta-diversity

display_name: beta-diversity

ecosystem-functions

display_name: ecosystem-functions

microbial-biodiversity

display_name: microbial-biodiversity

microbial-respiration

display_name: microbial-respiration

soil-respiration

display_name: soil-respiration

en: Chicken Creek 10 years


maintainer: Anita Risch

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

en: Datafile

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

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

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

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

Soil.moist	: Soil moisture (%)

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

pH: Soil pH

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

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

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

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

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

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

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

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

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

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

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

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

Plant.richness: Plant species richness

Plant.N: Plant tissue nitrogen content (%)

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

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

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

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

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

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

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

#References

- Anderson J, Domsch K. 1978. A physiological method for the quantitative measurement of microbial biomass in soil. Soil Biol Biochem 10:215–21.
- Blackwood CB, Marsh T, Kim S-H, Paul EA. 2003. Terminal Restriction Fragment Length Polymorphism Data Analysis for Quantitative Comparison of Microbial Communities. Appl Environ Microbiol 69:926–32. http://www.ncbi.nlm.nih.gov/pmc/articles/PMC143601/
- Bongers T. 1988. De nematoden von Nederland. Schoorl, The Netherlands: Pirola
- Byrnes JEK, Gamfeldt L, Isbell F, Lefcheck JS, Griffin JN, Hector A, Cardinale BJ, Hooper DU, Dee LE, Duffy JE. 2014. Investigating the relationship between biodiversity and ecosystem multifunctionality: Challenges and solutions. Methods Ecol Evol 5:111–24.
- Crossley DAJ, Blair JM. 1991. A high-efficiency low-technology Tulgren-type extractor for soil microarthopods. Agric Ecosyst Environ 34:187–92.
- Dudley N. 2008. Guidelines for applying protected area managment categories. Gland: IUCN
- Frank DA, McNaughton SJ. 1990. Aboveground biomass estimation with the canopy intercept method: A plant growth form caveat. Oikos 57:57–60.
- Haynes AG, Schütz M, Buchmann N, Page-Dumroese DS, Busse MD, Risch AC. 2014. Linkages between grazing history and herbivore exclusion on decomposition rates in mineral soils of subalpine grasslands. Plant Soil 374.
- Hodel M, Schütz M, Vandegehuchte ML, Frey B, Albrecht M, Busse MD, Risch AC. 2014. Does the aboveground herbivore assemblage influence soil bacterial community composition and richness in subalpine grasslands? Microb Ecol 68:584–95.
- Liu WT, Marsh TL, Cheng H, Forney LJ. 1997. Characterization of microbial diversity by determining terminal restriction fragment length polymorphisms of genes encoding 16S rRNA. Appl Environ Microbiol 63:4516–22. http://www.ncbi.nlm.nih.gov/pmc/articles/PMC168770/
- Manning P, van der Plas F, Soliveres S, Allan E, Maestre FT, Mace G, Whittingham MJ, Fischer M. 2018. Redefining ecosystem multifunctionality. Nat Ecol Evol 2:427–36. https://doi.org/10.1038/s41559-017-0461-7
- Meola M, Lazzaro A, Zeyer J. 2014. Diversity, resistance and resilience of the bacterial communities at two alpine glacier forefields after a reciprocal soil transplantation. Environ Microbiol 16:1918–34. https://onlinelibrary.wiley.com/doi/abs/10.1111/1462-2920.12435
- Meyer ST, Koch C, Weisser WW. 2015. Towards a standardized Rapid Ecosystem Function Assessment (REFA). Trends Ecol Evol 30:390–7. http://www.sciencedirect.com/science/article/pii/S0169534715000968
- Norman R., Stucki JW. 1981. The determination of nitrate and nitrite in soil extracts by ultraviolet spectrophotometry. Soil Sci Soc Am J 45:347–53.
- Ochoa-Hueso R. 2016. Non-linear disruption of ecological interactions in response to nitrogen deposition. Ecology 87:2802–2814.
- Oostenbrink M. 1960. Estimating nematode populations by some selected methods. In: Sasser NJ, Jenkins WR, editors. Nematology. Chapel Hill, NC, USA: University of North Carolina Press. pp 85–101.
- R Core Team. 2016. R: A language and environment for statistical computing. Vienna, Austria: R Foundation for Statistical Computing
- Risch AC, Haynes AG, Busse MD, Filli F, Schütz M. 2013. The response of soil CO2 fluxes to progressively excluding vertebrate and invertebrate herbivores depends on ecosystem type. Ecosystems 16:1192–202.
- Risch AC, Schütz M, Vandegehuchte ML, Van Der Putten WH, Duyts H, Raschein U, Gwiazdowicz DJ, Busse MD, Page-Dumroese DS, Zimmermann S. 2015. Aboveground vertebrate and invertebrate herbivore impact on net N mineralization in subalpine grasslands. Ecology 96:3312–22.
- Schütz M, Risch AC, Achermann G, Thiel-Egenter C, Page-Dumroese DS, Jurgensen MF, Edwards PJ. 2006. Phosphorus translocation by red deer on a subalpine grassland in the Central European Alps. Ecosystems 9:624–633.
- Schütz M, Risch AC, Leuzinger E, Krüsi BO, Achermann G. 2003. Impact of herbivory by red deer (Cervus elaphus L.) on patterns and processes in subalpine grasslands in the Swiss National Park. For Ecol Manage 181:177–88.
- Vandegehuchte ML, van der Putten WH, Duyts H, Schütz M, Risch AC. 2017a. Aboveground mammal and invertebrate exclusions cause consistent changes in soil food webs of two subalpine grassland types, but mechanisms are system-speciﬁc. Oikos 126:212–23.
- Vandegehuchte ML, Raschein U, Schütz M, Gwiazdowicz DJ, Risch AC. 2015. Indirect short- and long-term effects of aboveground invertebrate and vertebrate herbivores on soil microarthropod communities. PLoS One 10:e0118679.
- Vandegehuchte ML, Schütz M, de Schaetzen F, Risch AC. 2017b. Mammal-induced trophic cascades in invertebrate food webs are modulated by grazing intensity in subalpine grassland. J Anim Ecol 86:1434–46.
- Vandegehuchte ML, Trivellone V, Schütz M, Firn J, de Schaetzen F, Risch AC. 2018. Mammalian herbivores affect leafhoppers associated with specific plant functional types at different timescales. Funct Ecol 32:545–55.
- Wirthner S, Frey B, Busse MD, Schütz M, Risch AC. 2011. Effects of wild boar (Sus scrofa L.) rooting on the bacterial community structure in mixed-hardwood forest soils in Switzerland. Eur J Soil Biol 47:296–302. http://dx.doi.org/10.1016/j.ejsobi.2011.07.003
- Zumsteg A, Luster J, Göransson H, Smittenberg RH, Brunner I, Bernasconi SM, Zeyer J, Frey B. 2012. Bacterial, Archaeal and Fungal Succession in the Forefield of a Receding Glacier. Microb Ecol 63:552–64. https://doi.org/10.1007/s00248-011-9991-8

ecosystem-coupling

display_name: ecosystem-coupling

ecosystem-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: Ecosystem coupling and multifunctionality - exclosure experiment


maintainer: Alexandre Buttler

en: climate-change transplantation-experiment biogeochemisty soil silvopastoral-systems

en: Dataset

en: Zip archive of all datasets detailed in study.

mimetype: application/zip

en:
Silvopastoral systems are highly productive and combine long-term wood production with annual provision of forage for livestock. In the Swiss Jura Mountains these systems are a key component of the landscape. As in other cold biomes, climate change can potentially accelerate landscape change within these historically sustainable systems.

In order to anticipate the evolution of subalpine wooded pasture ecosystems under future climate and land-use changes, this project focused on the interplay between soil, vegetation and climate. It was aimed at providing experimental evidence for chief ecosystem processes, with emphasis on the quality of the ecosystem services provided. The main interest was placed on vegetation turf resistance to climate change along an unwooded – sparsely wooded - densely wooded pasture gradient (land-use intensity), where plant productivity, diversity and succession along with rates of carbon cycling and microbial activity provided measures of ecosystem functioning at both plot and landscape level.

Experimental transplantation of monolith soil turfs to lower altitudes allowed to simulate soil warming and reduced annual precipitation. In order to simulate a year-round warmer and drier climate the natural climate variation along an altitudinal gradient was used as a proxy. The aim was to simulate realistic climate change scenarios for the second half of the 21st century predicted by the IPCC report and downscaled for Switzerland providing regionalized interpolated projections integrating therein trends for temperature increase and precipitation decrease. By using permanent meteorological stations within the network of the Federal Office of Meteorology and Climatology (MeteoSwiss), we obtained high resolution regional data on the variation of mean annual temperature (MAT) and mean annual precipitation (MAP) in relation to altitude in the Swiss Jura Mountains. We observed a general increase of +0.5 K in MAT and a decrease of -20 % MAP for each 100 m decrease in altitude along the SE slope of the Swiss Jura Mountains. These relationships served for the selection of the transplantation sites such that in comparison to a control site at 1350 m a.s.l. (Combe des Amburnex, N 46°54’, E 6°23’) a +2 K MAT and -20 % MAP was achieved at 1010 m a.s.l. (Saint-George, N 46°52’, E 6°26’), a +4 K MAT and -40 % MAP at 570 m a.s.l., (Arboretum d’Aubonne, N 46°51’, E 6°37’), and a +5 K MAT and -50 % MAP at 395 m a.s.l. (Les Bois Chamblard, N 46°47’, E 6°41’). The two stations at 1010 m a.s.l. and 570 m a.s.l. corresponded to the IPCC scenario A1B for a moderate increase in greenhouse gas emissions and to scenario A2 for a high increase in greenhouse gas emissions, respectively. The station at 395 m a.s.l. was chosen to represent an extreme scenario with climate variables lying at the positive tail distribution of model predictions under the A2 scenario.

Soil cores were assembled into rectangular PVC boxes of 60  80 cm2 size and of 35 cm height. All mesocosms were dug down to surface level into previously prepared trenches in the ground thus preventing lateral heat exchange with the atmosphere. Since at each site the mesocosms were placed in a common garden with no light interception, mesocosms with turfs from the two wooded pastures were shaded from direct sun light to simulate the natural light conditions in the corresponding habitats. Each mesocosm was equipped with a drainage system and was connected to a water tank thus representing a zero potential lysimeter collecting soil solution and precipitation/snowmelt runoff. ECH2O EC-TM sensor probes coupled to Em50 data-loggers (Decagon Devices, Inc., USA) recorded soil temperature and volumetric water content in each mesocosm at the top-soil (0 to -3 cm) every minute and data were averaged over one hour intervals. Climate parameters at each transplantation site were monitored continuously throughout the experiment by means of automated weather stations (Sensor Scope Sàrl, Switzerland), measuring rain precipitation (non-heated tipping bucket gauges) and air temperature and humidity 2 m above the ground surface at one minute intervals.

A list of above- and belowground variables were measured to assess the resilience of biogeochemical processes, plant productivity, tree regeneration, and carbon sequestration for each respective land-use practice. Furthermore, the experimental data were used to improve on (parameterization) the existing spatially explicit, dynamic model WoodPaM and refine the modelʼs climatic and land-use variables so that different scenarios of climate change and land use change could be simulated. Natural and management induced disturbance patterns were incorporated into the model.
The data have been made available within the project CCES Mounted. The climate stations Sensorscope are still in use within the project CLIMARBRE (Wald und Klimawandel, WSL/BAFU).

#References

1. Puissant, J., Cécillon, L., Mills, R.T.E., Robroek, B.J.M. Gavazov, K., De Danieli, S., Spiegelberger, T., Buttler, A., Brun, J.J. 2015. Seasonal influence of climate manipulation on microbial community structure and function in mountain soils. Soil Biology and Biochemistry 80: 296–305.
2. Mills, R., K. Gavazov, T. Spiegelberger, D. Johnson and A. Buttler 2014. Diminished soil functions occur under simulated climate change in a sup-alpine pasture, but heterotrophic temperature sensitivity indicates microbial resilience. Science of the Total Environment, vol. 473–474(0): 465-472.
3. Gavazov, K., Spiegelberger, T. and Buttler, A. 2014. Transplantation of subalpine wood-pasture turfs along a natural climatic gradient reveals lower resistance of unwooded pastures to climate change compared to wooded ones. Oecologia (174) : 1425-1435.
4. Peringer A., Siehoff S., Chételat J., Spiegelberger T., Buttler A. & Gillet F. 2013. Past and future landscape dynamics in pasture-woodlands of the Swiss Jura Mountains under climate change. Ecology and Society, 18, 3: 11. DOI: 10.5751/ES-05600-180311. [online] URL: http://www.ecologyandsociety.org/vol18/iss3/art11/
5. Gavazov, K. S., A. Peringer, A. Buttler, F. Gillet and T. Spiegelberger. 2013. Dynamics of Forage Production in Pasture-woodlands of the Swiss Jura Mountains under Projected Climate Change Scenarios. Ecology and Society 18 (1): 38. [online] URL: http://www.ecologyandsociety.org/vol18/iss1/art38/

biogeochemisty

display_name: biogeochemisty

climate-change

display_name: climate-change

silvopastoral-systems

display_name: silvopastoral-systems

soil

display_name: soil

transplantation-experiment

display_name: transplantation-experiment

educ

en: Education, culture and sport

envidat

en: EnviDat: the Environmental Data Portal

en: Biogeochemical data from a transplantation experiment of monolith soil turfs along an altitudinal gradient to simulate climate change scenarios


en: isotopes pinus-sylvestris scots-pine tree-rings tree-ring-cellulose pfynwald dendrochronology

media_type: text/csv

en: Isotope measurements of tree-level tissues for the vegetative season 2019.

format: CSV

en: Read me file.docx

en:
Data from a 17-year-long irrigation experiment (Pfynwald, Switzerland) in a naturally dry forest dominated by 100-year-old pine trees (Pinus sylvestris). This dataset includes measure tree-ring width and tree-ring isotope chronologies (stable isotope ratios of non-exchangeable hydrogen δ2H, oxygen δ18O, and carbon δ13C), for the Pfynwald experiment, including control trees, irrigation and irrigation-stop treatments until the year 2019.

This dataset contains all data on which the following publication below is based.
Please cite this paper together with the citation for the datafile.

dendrochronology

display_name: dendrochronology

isotopes

display_name: isotopes

pfynwald

display_name: pfynwald

pinus-sylvestris

display_name: pinus-sylvestris

scots-pine

display_name: scots-pine

tree-ring-cellulose

display_name: tree-ring-cellulose

tree-rings

display_name: tree-rings

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: Pfynwald 2019 - Dendrochronological and tree-ring isotope dataset


maintainer: EnviDat Support

en: snow acoustic-emissions snow-mechanics sintering fiber-bundle-model snow-avalanche snow-failure viscous-deformation

en: fiber-bundle-model-for-snow-failure

en: Data underlying Figures in publication "Modelling Snow Failure Behavior and Concurrent Acoustic Emissions Signatures with a Fiber Bundle Model" submitted to "Geophysical Research Letters"

en:
This dataset contains modeled and experimental results for laboratory snow failure experiments and the concurrent acoustic emissions signatures for different loading rates. For modelling the snow failure we used a fiber bundle model that includes sintering and viscous deformation.

The data underlay the figures in the publication "Modelling Snow Failure Behavior and Concurrent Acoustic Emissions Signatures with a Fiber Bundle Model" submitted for publication to "Geophysical Research Letters".

acoustic-emissions

display_name: acoustic-emissions

fiber-bundle-model

display_name: fiber-bundle-model

sintering

display_name: sintering

snow

display_name: snow

snow-avalanche

display_name: snow-avalanche

snow-failure

display_name: snow-failure

snow-mechanics

display_name: snow-mechanics

viscous-deformation

display_name: viscous-deformation

en: Fiber Bundle Model for snow failure and concurrent Acoustic Emissions


en: madagascar landscape-evolution geology endemism flora

en: Data v1.0

en: used for paper submission only

en: Escarpment evolution drives the diversification of the Madagascar flora

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

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

endemism

display_name: endemism

flora

display_name: flora

geology

display_name: geology

landscape-evolution

display_name: landscape-evolution

madagascar

display_name: madagascar


bryophytes-of-europe-traits-bet-dataset

title_for_slug: bryophytes-of-europe-traits-bet-dataset

en: bioclimatic-variables indicator-values life-history-traits red-list liverworts iucn hornworts mosses

media_type: text/plain

en: Text file including the BET dataset.

format: TXT

en: Excel file including the BET dataset and (trait) explanations.

media_type: application/pdf

en: PDF including the (trait) explanations.

format: PDF

en: The Bryophytes of Europe Traits (BET) dataset includes values for 65 biological and ecological traits and 25 bioclimatic variables for all 1816 bryophytes included in the European Red List (Hodgetts et al. 2019). The traits are compiled from several regional trait datasets and manually complemented using Floras, species-specific literature and expert knowledge. The bioclimatic variables are calculated using the European range of each species. Details regarding the trait compilation and extraction of bioclimatic variables can be found in the corresponding data paper (Van Zuijlen et al. 2023).

bioclimatic-variables

display_name: bioclimatic-variables

hornworts

display_name: hornworts

indicator-values

display_name: indicator-values

iucn

display_name: iucn

life-history-traits

display_name: life-history-traits

liverworts

display_name: liverworts

mosses

display_name: mosses

red-list

display_name: red-list

educ

en: Education, culture and sport

envidat

en: EnviDat: the Environmental Data Portal


maintainer: Marco Moretti

en: urbanization zurich honeybees bettergardens city4bees gardens wild-bees urban-ecosystems resource-availability beekeeping urban-biodiversity pollinator-experiment

en: Metadata for the predictors and response dataset

en:
The data contains the following columns:

  SiteID: numeric, the identity of the garden where the bee was sampled.
  Taxonname: character, species name
  Lecty: numeric discreet, a mesure of specialisation degree. Levels: 1 = monolectic; 2=oliolectic; 3=polilectic
  Pheno.start= numeric discreet, the starting week of the flying activity.
  Pheno.end= numeric discreet, the ending week of the flying activity.
  Pheno.duration=numeric discreet, Pheno.end - Pheno.start
  Daytime.activity = numeric continuous, individual-level measure of the day hour when the bee was sampled
  ITD = numeric continuous, individual-level measure of the InterTegular Distance, a metric of mobility in mm.
  Rel.tongue.length =numeric continuous, individual-level measure of the relative tongue length (Tongue length / ITD), a metric of specilaisation degree, in mm.

en: Metadata for the predictor and response dataset

en: Response and predictors used for the SEMs

en:
Mean, standard deviation , minimum and maximum values of six functional traits. The data has the following structure:
- Bee_species: bee scientific name
- mean_trait: mean value
- sd_trait: standard deviation
_min_trait: minimum value
- max_trait: maximum value
- trait: the six traits used. ITD = Intertegular distance (mm); Pheno.duration = duration of the phenology; Pheno.start = start of the phenology; Pheno.end = end of the phenology; Rel.tongue.length= relative tongue length (mm); Daytime.activity = daily activity (h)
DistNichePart: functional dissimilarity in a multidimentional trait space defined by five traits between wild bee individuals of a wild bee species and the honeybee individuals. Values are at the species level.

en:
Cities are socio-ecological systems that filter and select species, thus establishing unique species assemblages and biotic interactions. Urban ecosystems can host richer wild bee communities than highly intensified agricultural areas, specifically in resource-rich urban green spaces such as allotment and family gardens. At the same time, urban beekeeping has boomed in many European cities, raising concerns that the fast addition of a large number of managed bees could deplete the existing floral resources, triggering competition between wild bees and honeybees. The data has been used to investigated the interplay between resource availability and the number of honeybees at local and landscape scales and how this relationship influences wild bee diversity.

This dataset contains the raw and processed data supporting the findings from the paper: "Low resource availability drives feeding niche partitioning between wild bees and honeybees in a European city".

The data contains:
1. Bee trait measurements at the species and individual-level of five functional traits.
2. The values of the feeding niche partitioning (functional dissimilarity to honeybees)
3. The predictors of resource availability and beekeeping intensity at local and landscape scales used in the modelling of the paper for the 23 experimental sites.

beekeeping

display_name: beekeeping

bettergardens

display_name: bettergardens

gardens

display_name: gardens

honeybees

display_name: honeybees

pollinator-experiment

display_name: pollinator-experiment

resource-availability

display_name: resource-availability

urban-biodiversity

display_name: urban-biodiversity

urban-ecosystems

display_name: urban-ecosystems

urbanization

display_name: urbanization

wild-bees

display_name: wild-bees

zurich

display_name: zurich

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: Niche partitioning between wild bees and honeybees


aerosol-data-davos-wolfgang

title_for_slug: aerosol-data-davos-wolfgang

en: raclets aerosol inp ice-nucleation drincz particles

en: SMPS Dataset Davos Wolfgang

en: The SMPS file contains aerosol data (particle concentration, total number concentration, median, mean, geometric mean, mode and geometric standard deviation of the size distribution) in a size range between 12 and 460 nm (electrical mobility diameter) as well as instrument characteristics (sample temperature, pressure, relative humidity, mean free path and gas viscosity), in a temporal resolution of 2 minutes, with time in UTC, measured at Davos Wolfgang.

mimetype: application/x-netcdf

en: OPC GT-526S Dataset Davos Wolfgang

en: Particle counts were recorded in six size channels (0.3, 0.5, 0.8, 1.5, 2.5 and 5 μm) in a resolution of 20 seconds (time in UTC) by a particle counter (GT-526S, Met One Instruments, Inc.).

mimetype: text/csv

en: OPC-N3 Dataset Davos Wolfgang

en: Particle concentrations in a size range of 0.35 μm to 40 μm were measured with an OPC-N3 (Alphasense, Inc.) in a resolution of 20 seconds (time in UTC). PM₁, PM₂,₅ and PM₁₀ were directly derived.

en: APS Dataset Davos Wolfgang

en: The APS file contains aerosol data (total number concentration, median, mean, geometric mean, mode and geometric standard deviation of the size distribution) for aerodynamic diameters between 0.5 μm and ~20 μm as well as instrument characteristics, in a temporal resolution of 20 seconds, with time in UTC, measured at Davos Wolfgang.

en: DRINCZ Dataset Davos Wolfgang

en: The DRINCZ file contains information on temperature (in °C) dependent frozen fractions, number of Ice Nuleating Particles (INP, per standard liter) and differential INP concentrations (per standard liter and Kelvin).

en:
Aerosol properties were measured between February 8 and March 31 2019 at the measurement site Davos Wolfgang (LON: 9.853594, LAT: 46.835577). Optical and aerodynamic particle counters, as well as a scanning mobility particle size spectrometer and an ice nuclei counter were deployed to report particle concentrations and size distributions in fine (10-1000 nm) and coarse mode (> 1000 nm), cloud condensation nuclei concentrations (CCNCs) and ice nuclei particle concentrations (ICNCs). The ambient particles were transported via a heated inlet to be distributed to the particle detecting devices inside the setup room.

Optical Particle Counter (OPC): Light scattering of a diode laser beam caused by travelling particles is used in the both, the OPC-N3 (0.41 - 38.5 μm) and GT-526S (0.3 – 5 μm), to determine their size and number concentration. For the OPC-N3, particle size spectra and concentration data are used afterwards to calculate PM₁, PM₂,₅ and PM₁₀ (assumptions: particle density: 1.65 g cmˉ³, refractive index: 1.5+i0).

Aerodynamic Particle Sizer (APS): The APS (3321, TSI Inc.) measured the particle size distribution for aerodynamic diameters between 0.5 μm and ~20 μm by the particle’s time-of-flight and light-scattering intensity (assumptions: particle density 1 g cmˉ³).

Scanning Mobility Particle Size Spectrometer (SMPS): Particle number concentrations in a size range between 12 and 460 nm (electrical mobility diameter) were measured at Davos Wolfgang, using a Scanning Mobility Particle Sizer Spectrometer (3938, TSI Inc.). The classifier (3082, TSI Inc.) was equipped with a neutralizer (3088, TSI Inc.) and a differential mobility analyzer working with negative polarity (3081, TSI Inc.). The size selected particles were counted by a water-based condensation particle counter (3788 , TSI Inc.). The TSI AIM software was used to provide particle size distributions by applying multiple charge and diffusion loss corrections (assumptions: particle density 1 g cmˉ³).

Coriolis μ and DRINCZ: A microbial air sampler (Coriolis μ, bertin Instruments) was used to collect airborne particles for investigating their ice nucleating ability with a droplet freezing device. Particles larger than 0.5 μm were drawn with an air flow rate of up to 300 l minˉ¹ into the cone and centrifuged into the wall of the cone due to the forming vortex. The liquid sample was transferred into the DRoplet Ice Nuclei Counter Zurich (DRINCZ, ETH Zurich) to study heterogeneous ice formation (immersion freezing mode) of ambient airborne particles.

aerosol

display_name: aerosol

drincz

display_name: drincz

ice-nucleation

display_name: ice-nucleation

inp

display_name: inp

particles

display_name: particles

raclets

display_name: raclets

en: Aerosol Data Davos Wolfgang


maintainer: Sofia Pagliarin

en: milan barcelona imperviousness urban-atlas copernicus soil-sealing

en: Information on data sources

en: Shareable project in Esri ArcGIS format including the HRL IMD data in raster format for each of the territorial boundaries as specified in letter a)-h), see Dataset description

en:
Dataset description

This dataset is a recalculation of the Copernicus 2015 high resolution layer (HRL) of imperviousness density data (IMD) at different spatial/territorial scales for the case studies of Barcelona and Milan. The selected spatial/territorial scales are the following:

 * a)	Barcelona city boundaries
 * b)	Barcelona metropolitan area, Àrea Metropolitana de Barcelona (AMB)
 * c)	Barcelona greater city (Urban Atlas)
 * d)	Barcelona functional urban area (Urban Atlas)
 * e)	Milan city boundaries
 * f)	Milan metropolitan area, Piano Intercomunale Milanese (PIM)
 * g)	Milan greater city (Urban Atlas)
 * h)	Milan functional urban area (Urban Atlas)

In each of the spatial/territorial scales listed above, the number of 20x20mt cells corresponding to each of the 101 values of imperviousness (0-100% soil sealing: 0% means fully non-sealed area; 100% means fully sealed area) is provided, as well as the converted measure into squared kilometres (km2).

 Dataset composition

The dataset is provided in .csv format and is composed of:

_IMD15_BCN_MI_Sources.csv_: Information on data sources

 _IMD15_BCN.csv_: This file refers to the 2015 high resolution layer of imperviousness density (IMD) for the selected territorial/spatial scales in Barcelona:
 * a)	Barcelona city boundaries (label: bcn_city)
 * b)	Barcelona metropolitan area, Àrea metropolitana de Barcelona (AMB) (label: bcn_amb)
 * c)	Barcelona greater city (Urban Atlas) (label: bcn_grc)
 * d)	Barcelona functional urban area (Urban Atlas) (label: bcn_fua)

 _IMD15_MI.csv_: This file refers to the 2015 high resolution layer of imperviousness density (IMD) for the selected territorial/spatial scales in Milan:
 * e)	Milan city boundaries (label: mi_city)
 * f)	Milan metropolitan area, Piano intercomunale milanese (PIM) (label: mi_pim)
 * g)	Milan greater city (Urban Atlas) (label: mi_grc)
 * h)	Milan functional urban area (Urban Atlas) (label: mi_fua)

_IMD15_BCN_MI.mpk_: the shareable project in Esri ArcGIS format including the HRL IMD data in raster format for each of the territorial boundaries as specified in letter a)-h).

Regarding the territorial scale as per letter f), the list of municipalities included in the Milan metropolitan area in 2016 was provided to me in 2016 from a person working at the PIM.

In the IMD15_BCN.csv and IMD15_MI.csv, the following columns are included:

 * Level: the territorial level as defined above (a)-d) for Barcelona and e)-h) for Milan);
 * Value: the 101 values of imperviousness density expressed as a percentage of soil sealing (0-100%: 0% means fully non-sealed area; 100% means fully sealed area);
 * Count: the number of 20x20mt cells corresponding to a certain percentage of soil sealing or imperviousness;
 * Km2: the conversion of the 20x20mt cells into squared kilometres (km2) to facilitate the use of the dataset.

 Further information on the Dataset

This dataset is the result of a combination between different databases of different types and that have been downloaded from different sources. Below, I describe the main steps in data management that resulted in the production of the dataset in an Esri ArcGIS (ArcMap, Version 10.7) project.

 1. The high resolution layer (HRL) of the imperviousness density data (IMD) for 2015 has been downloaded from the official website of Copernicus. At the time of producing the dataset (April/May 2021), the 2018 version of the IMD HRL database was not yet validated, so the 2015 version was chosen instead. The type of this dataset is raster.

 2. For both Barcelona and Milan, shapefiles of their administrative boundaries have been downloaded from official sources, i.e. the ISTAT (Italian National Statistical Institute) and the ICGC (Catalan Institute for Cartography and Geology). These files have been reprojected to match the IMD HRL projection, i.e. ETRS 1989 LAEA.

 3. Urban Atlas (UA) boundaries for the Greater Cities (GRC) and Functional Urban Areas (FUA) of Barcelona and Milan have been checked and reconstructed in Esri ArcGIS from the administrative boundaries files by using a Eurostat correspondence table. This is because at the time of the dataset creation (April/May 2021), the 2018 Urban Atlas shapefiles for these two cities were not fully updated or validated on the Copernicus Urban Atlas website. Therefore, I had to re-create the GRC and FUA boundaries by using the Eurostat correspondence table as an alternative (but still official) data source. The use of the Eurostat correspondence table with the codes and names of municipalities was also useful to detect discrepancies, basically stemming from changes in municipality names and codes and that created inconsistent spatial features. When detected, these discrepancies have been checked with the ISTAT and ICGC offices in charge of producing Urban Atlas data before the final GRC and FUA boundaries were defined.

Steps 2) and 3) were the most time consuming, because they required other tools to be used in Esri ArcGIS, like spatial joins and geoprocessing tools for shapefiles (in particular dissolve and area re-calculator in editing sessions) for each of the spatial/territorial scales as indicated in letters a)-h).

Once the databases for both Barcelona and Milan as described in points 2) and 3) were ready (uploaded in Esri ArcGIS, reprojected and their correctness checked), they have been ‘crossed’ (i.e. clipped) with the IMD HRL as described in point 1) and a specific raster for each territorial level has been calculated. The procedure in Esri ArcGIS was the following:

 * Clipping: Arctoolbox > Data management tools > Raster > Raster Processing > Clip. The ‘input’ file is the HRL IMD raster file as described in point 1) and the ‘output’ file is each of the spatial/territorial files. The option "Use Input Features for Clipping Geometry (optional)” was selected for each of the clipping.
 * Delete and create raster attribute table: Once the clipping has been done, the raster has to be recalculated first through Arctoolbox > Data management tools > Raster > Raster properties > Delete Raster Attribute Table and then through Arctoolbox > Data management tools > Raster > Raster properties > Build Raster Attribute Table; the "overwrite" option has been selected.

 Other tools used for the raster files in Esri ArcGIS have been the spatial analyst tools (in particular, Zonal > Zonal Statistics). As an additional check, the colour scheme of each of the newly created raster for each of the spatial/territorial attributes as per letters a)-h) above has been changed to check the consistency of its overlay with the original HRL IMD file. However, a perfect match between the shapefiles as per letters a)-h) and the raster files could not be achieved since the raster files are composed of 20x20mt cells.

The newly created attribute tables of each of the raster files have been exported and saved as .txt files. These .txt files have then been copied in the excel corresponding to the final published dataset.

barcelona

display_name: barcelona

copernicus

display_name: copernicus

imperviousness

display_name: imperviousness

milan

display_name: milan

soil-sealing

display_name: soil-sealing

urban-atlas

display_name: urban-atlas

educ

en: Education, culture and sport

envidat

en: EnviDat: the Environmental Data Portal

en: Soil sealing Barcelona and Milan different territorial levels


en: borehole permafrost permos ritigraben ground-temperature

en: Map of PERMOS borehole network

en: DATA ACCESS

en: PERMOS DATA POLICY

en:
_ENVIDAT NOTE: Data currently unvailable and measures are being taken to recover and restore the data files._

Processed ground temperature measurements at the Ritigraben permafrost borehole (RIT_0102) in canton Valais, Switzerland. The borehole is located at 2690 m asl on a flat site. The surface material is coarse blocks and borehole depth is 30 m. Thermistors used YSI 44006. Year of drilling 2002. This borehole is part of the Swiss Permafrost network, PERMOS (www.permos.ch). Contact phillips@slf.ch for details of processing applied.

borehole

display_name: borehole

ground-temperature

display_name: ground-temperature

permafrost

display_name: permafrost

permos

display_name: permos

ritigraben

display_name: ritigraben

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: RIT1: Processed permafrost borehole data (2690  m asl), Ritigraben, Switzerland


en: force remote-sensing sentinel-2 raster-processing switzerland

en: An example of the index EVI for one of the generated 30 by 30 km tiles located around the city of Zürich. The values are multiplied by 10.000. The date of the image is 24.07.2018.

en:
We processed Sentinel-2 images from 2017 to 2023 for Switzerland with the Software FORCE (Frantz 2019). The respective parameter files can be found here: [Github](https://github.com/TLKoch/Sentinel-2_CH). All the images consist of several TB and therefore, access will be granted upon request.
The available bands (in spatial reference system EPSG 3035) are the following:
*Red, Green, Blue, NIR, Red-Edge-1, Red-Edge-2, Red-Edge-3, SWIR-1, SWIR-2*
The available indices (in spatial reference system EPSG 3035) are the following:
*CCI, CIRE, NDWI/NDMI, NDVI, EVI*
Further indices might be provided upon request.

 Processing
After downloading Level 1 data for the 14 Sentinel-2 tiles covering Switzerland (T31TGN, T32TLT, T32TMT, T32UMU, T32TNT, T32TPT, T31TGM, T32TLS, T32TMS, T32TNS, T32TPS, T32TLR, T32TMR, T32TNR) with an estimated cloud cover of less than 80 \%, we processed the data further with FORCE v. 3.7.8-12.
FORCE was used for radiometric correction, including atmospheric and topographic corrections using the digital elevation model from Copernicus Land Monitoring Service (EU-DEM v. 1.1), with a 25 m spatial resolution, a bidirectional reflectance distribution function (BRDF) correction, and an adjacency effect correction. For cloud masking, the improved Fmask algorithm with buffers of 300 m for clouds, 90 m for shadows, and 30 m for snow were used (Frantz et al. 2018; Zhu et al. 2015). All bands were resampled using cubic convolution to 10 m spatial resolution. Shadows, low and poor illumination as well as saturation were masked out. The co-registration of all images was made with monthly composites of near-infrared Landsat Collection 2 images from 2014 to 2021 (Rengarajan et al. 2020;Rufin et al. 2021). With this the geometric consistency improved. The processed images are available in tiles of 30 by 30 km.

 Example images
Uploaded is an example of the index EVI for one of the generated 30 by 30 km tiles located around the city of Zürich. The values are multiplied by 10.000. The date of the image is 24.07.2018.

force

display_name: force

raster-processing

display_name: raster-processing

remote-sensing

display_name: remote-sensing

switzerland

display_name: switzerland

en: Sentinel-2 imagery of Switzerland


en: decision-making hydrology estimation-methods engineering flood

en:
(English version below)
Ziel dieser Faktenblätter ist es Informationen zu den Schätzmethoden, Hinweise zur Parametrisierung und eine grobe Einschätzung der Güte der Resultate in übersichtlicher Form bereitzustellen. Ein zeitaufwändiges Zusammensuchen dieser Informationen aus unterschiedlichen Quellen entfällt daher weitgehend. Die Bearbeitenden sollen damit in der Lage sein, sich innerhalb weniger Minuten die wichtigsten Hintergrundinformationen zu jeder der vorgestellten Methoden in Erinnerung zu rufen. Der Leitfaden unterstützt bei der Plausibilisierung und bei der Mittelung der Ergebnisse der einzelnen Schätzmethoden zu einem repräsentativen Endergebnis. Vorausgesetzt wird Grundwissen und Erfahrung in der Thematik.
Der Leitfaden führt die Fachperson anhand eines Entscheidungsbaums in acht Schritten durch den Arbeitsablauf und unterstützt mit einem Fragenkatalog bei der Plausibilisierung der Ergebnisse.
Auf den Faktenblättern sind für jede Schätzmethode alle relevanten Informationen stichwortartig und grafisch übersichtlich auf einer DIN-A4 Seite zusammengefasst. Jedes Faktenblatt ist einheitlich gegliedert.
The aim of these fact sheets is to provide information on the flood estimation methods, notes on their parameterization and a rough assessment of the quality of the results in a clear form. A time-consuming research for this information from different sources is therefore largely eliminated. The users should be able to recall the most important background information on each of the methods presented within a few minutes. The guide provides support in checking plausibility and averaging the results of the individual estimation methods to produce a representative final result. Basic knowledge and experience in the subject are assumed.
The guide leads the expert through the workflow in eight steps using a decision tree and supports the plausibility check of the results with a list of questions.
On the fact sheets, all relevant information for each estimation method is summarized with key words and graphics on one DIN A4 page. Each fact sheet has a standardized structure.

decision-making

display_name: decision-making

engineering

display_name: engineering

estimation-methods

display_name: estimation-methods

flood

display_name: flood

hydrology

display_name: hydrology

en: Faktenblätter und Leitfaden für Hochwasserschätzmethoden in der Praxis


en: weissfluhjoch ice-layers snowmicropen snow-temperature water-front snow-stratigraphy

en: README

mimetype: text/plain

en: WFJ_ICE_LAYERS dataset

en: The WFJ_ICE_LAYERS dataset contains multi-instrument snowpack measurements at high temporal resolution, which enable to monitor the formation of deep ice layers due to preferential water flow, at the Weissfluhjoch research site, Davos, Switzerland. It covers the winter 2016/2017, with a focus on the early melting season. This dataset includes traditional snowpack profiles (weekly resolution, 15/11/2016-29/05/2017), SnowMicroPen penetration resistance profiles (daily resolution, 01/02/2017-19/04/2017), snow temperatures measured at different heights in the snowpack (half-hourly resolution, 01/03/2017-15/04/2017) and the water front height derived from an upward-looking ground penetrating radar (3-hour resolution, 04/03/2017-08/04/2017). The measurements are complemented by initialization files for SNOWPACK model simulations with the ice reservoir parameterization at Weissfluhjoch for the winter 2016/2017.

ice-layers

display_name: ice-layers

snow-stratigraphy

display_name: snow-stratigraphy

snow-temperature

display_name: snow-temperature

snowmicropen

display_name: snowmicropen

water-front

display_name: water-front

weissfluhjoch

display_name: weissfluhjoch

educ

en: Education, culture and sport

en: WFJ_ICE_LAYERS: Multi-instrument data for monitoring deep ice layer formation in an alpine snowpack


maintainer: Matthias Haeni

en: swiss-forest-lab meteo long-term precipitation temperature climate-change wind-speed relative-humidity par meteorology

en: Data plot of the forest station (ALB)

en: Data overview for air temperature, relative humidity, precipitation, PAR, wind speed.

mimetype: application/pdf

en: Forest station data (ALB)

en: Site aerial photo (Alpthal)

en: Site aerial photo from the Alpthal forest station. Source: Google. 2016. Site aerial photo from the Alpthal forest station. Retrieved November 11, 2016, from https://www.google.ch/maps

mimetype: image/jpeg

en: High quality meteorological data are needed for long-term forest ecosystem research, particularly in the light of global change. The long-term data series published here comprises almost 20 years of measurements for one meteorological station in Alpthal in Switzerland which is located within a natural coniferous forest (ALB) with Norway spruce (_Picea abies_; 180-230 yrs) as dominant tree species. The meteorological time series are presented in hourly time resolution of air temperature, relative humidity, precipitation, photosynthetically active radiation (PAR) and wind speed. Alpthal is part of the Long-term Forest Ecosystem Research Programme (LWF) established and maintained by the Swiss Federal Research Institute WSL.

climate-change

display_name: climate-change

long-term

display_name: long-term

meteo

display_name: meteo

meteorology

display_name: meteorology

par

display_name: par

precipitation

display_name: precipitation

relative-humidity

display_name: relative-humidity

swiss-forest-lab

display_name: swiss-forest-lab

temperature

display_name: temperature

wind-speed

display_name: wind-speed

envidat

en: EnviDat: the Environmental Data Portal

en: Alpthal, Switzerland: Long-term forest meteorological data from the Long-term Forest Ecosystem Research Programme (LWF), from 1997 onwards


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

en: Wetlands 1850 - 2010 (shapefiles)

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

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

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

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

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

ecology

display_name: ecology

environmental---history

display_name: environmental---history

environmental--policy

display_name: environmental--policy

historical-carthography

display_name: historical-carthography

switzerland

display_name: switzerland

wetlands

display_name: wetlands

en: 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: History of wetlands in Switzerland since 1850


maintainer: Jana von Freyberg

en: hydrology stable-water-isotope stream-water precipitation catchment alptal

en: Data Set Documentation: alptal_Isotopes_daily_2015-2019_v2

en: Documentations contains meta data of the data columns and information about the study catchments.

en: Single comma-separated txt-file with daily data of stable water isotopes measured in streamwater and precipitation in the Swiss Alptal catchment and two of its tributaries (Erlenbach and Vogelbach), as well as daily data of key hydrometeorological variables from the Alptal valley

en:
Version 2 of the dataset contains additional information on:
- line-conditioned (lc) excess
- precipitation sample volumes
- isotope data quality

en: This dataset contains four years of daily measurements of the natural isotopic composition (2H, 18O) of precipitation and stream water at the Alp catchment (area 47 km2) in Central Switzerland and two of its tributaries (0.73 km2 and 1.55 km2). In addition, the dataset contains daily measurements of key hydrometeorological variables.

alptal

display_name: alptal

catchment

display_name: catchment

hydrology

display_name: hydrology

stable-water-isotope

display_name: stable-water-isotope

stream-water

display_name: stream-water

educ

en: Education, culture and sport

en: Four years of daily stable water isotope data in stream water and precipitation from three Swiss catchments


en: cces pore-water tramm pressure-perturbations landslides landslide-testsite

en: TRAMM Ruedlingen data

en: TRAMM project data from the Ruedlingen site (exp 1 + 2). Measured parameters include soil suction, water level, soil volumetric water content, rain intensity, and soil temperature.

en:
A landslide testsite dataset related to pore water pressure perturbations on the stability of unsaturated silty sand slopes leading to the initiation and propagation of the shear deformations and eventual rapid mass movements. This project was initiated and led by the Institute of Geotechnical Engineering (IGT) of the Swiss Federal Institute of Technology (ETH Zurich) and was incorporated in a Swiss national (TRAMM) and a European Union (SafeLand) multidisciplinary research project. Field site: The experimental slope is 7.5 m wide by 35 m long, located in the Swiss lowlands on an east facing slope over-looking the river Rhine, at an altitude of ~ 350 masl. Originally there were forestry covertures of circa 80%, heights of 5-20 m. Shrubs up to 1-5 m high and a free herb layer covered ~ 50% of the surface. The average gradient was determined to be from 38° to 43° with a slightly concave surface. The underlying rock consists mainly of Molasse, which is formed by alternate layers of sea deposits under the Tethys Sea (Seawater Molasse) and land deposits (Freshwater Molasse). Several augured samples, as well as an outcrop of the bedrock about 20 m above the selected field, revealed horizontal layering of fine grained sand- and marlstone at the test site. The sandstone was later proven to be highly permeable and fissured. Grain-size distributions were determined and the soil was classified as medium-low plasticity silty sand. Site instrumentation:Measurements of soil suction, groundwater level, soil volumetric water content, rain intensity and soil temperature were taken and combined with geophysical monitoring using Electrical Resistance Tomography (ERT) and investigations into subsurface flow by means of tracer experiments. Deformations were monitored during the experiment, both on the surface via photogrammetrical methods and within the soil mass, using a flexible probe equipped with strain gauges at different points and two axis inclinometers on the top and acoustic sensors. Instruments were installed mainly in three clusters at depths of 15, 30, 60, 90, 120, and 150 cm below the ground surface over the slope, including jet-fill tensiometers, TDRs, Decagon TDRs, piezometers, soil temperature sensors, deformation probes, earth pressure cells, acoustic sensors and rain gauges. A ring-net barrier (provided by Geobrugg AG) was set up at the foot of the slope to protect the road. Experiments: A sprinkling experiment was carried out in September 2008 to investigate the hydrological and mechanical response of the slope (Experiment 1), followed by a second one to trigger a landslide in March 2009 (Experiment 2).

Publications

1. Lehmann, P., F. Gambazzi, B. Suski, L. Baron, A. Askarinejad, S. M. Springman, K. Holliger, and D. Or (2013), Evolution of soil wetting patterns preceding a hydrologically induced landslide inferred from electrical resistivity survey and point measurements of volumetric water content and pore water pressure, Water Resour. Res., 49, 7992–8004, doi:[10.1002/2013WR014560](http://dx.doi.org/10.1002/2013WR014560).

2. Springman, S. M., Kienzler, P., Casini, F., & Askarinejad, A. (2009). Landslide triggering experiment in a steep forested slope in Switzerland. In 17th International Conference of Soil Mechanics and Geotechnical Engineering, Alexandria, Egypt (pp. 1698-1701). doi: [10.3233/978-1-60750-031-5-1698](http://dx.doi.org/10.3233/978-1-60750-031-5-1698)

cces

display_name: cces

landslide-testsite

display_name: landslide-testsite

landslides

display_name: landslides

pore-water

display_name: pore-water

pressure-perturbations

display_name: pressure-perturbations

tramm

display_name: tramm

en: TRAMM project Ruedlingen experimental landslide dataset, Switzerland