maintainer: Armin Sigmund

en: backward-trajectories snow-sublimation antarctica isotopic-distillation evaporation lagrangian-analysis stable-water-isotopes

en: Model code

en: Model Sublimation and Model Air Parcel (python scripts)

en: Python scripts for data visualization

en: Scripts for generating the figures of the related research article and generating the data files (csv) from the model output

en: Data

en: Modeled data including the data shown in the figures of the related research article

en:
 Summary

This data set contains Python programming code and modeled data discussed in a related research article. We developed a simple isotope model to study the drivers of the particularly depleted vapour isotopic composition measured on the ship of the Antarctic Circumnavigation Expedition close to the outlet of the Mertz glacier, East Antarctica, in the 6-day period from 27 January 2017 to 1 February 2017. The model considers the stable water isotopologues H2(16O), H2(18O), and HD(16O). It uses data from the ERA5 reanalysis product with a spatial resolution of 0.25° x 0.25° (Hersbach et al., 2018) and 10-day backward trajectories for the location of the ship, published by Thurnherr et al. (2020a). Our data set includes the model code, Python scripts for visualizing the results, and data produced by the model including the results shown in the figures of the related research article. Here, we summarize the most important model characteristics while further details can be found in the readme.txt file and the related research article including its supporting information.

 Main model characteristics

The modeling approach consists of two steps called *Model Sublimation* and *Model Air Parcel*. The former estimates the isotopic compositions of the snow and sublimation flux across the Antarctic Ice Sheet using an Eulerian frame of reference while the latter models the vapour isotopic composition and specific humidity along air parcel trajectories using a Lagrangian frame of reference. The isotope effects of most phase changes are represented by equilibrium fractionation. Only for ocean evaporation, kinetic fractionation is additionally taken into account (original Craig-Gordon formula). For snow sublimation, two assumptions are tested: *Run E* assumes that sublimation is associated with equilibrium fractionation while *Run N* assumes that sublimation occurs without isotopic fractionation.

 Model Sublimation
Model Sublimation uses a simple one-dimensional mass-balance approach in each grid cell, considering snow accumulation due to snowfall and vapour deposition and snow ablation due to sublimation. The snowpack is represented by 100 layers of equal thickness (e.g., 1 cm) and density (350 kg m-3). The isotopic composition of snowfall is parameterized by generalizing a site-specific, empirical relationship between the daily mean air temperature and snowfall isotopic composition. In the case of vapour deposition, Model Sublimation assumes equilibrium fractionation and estimates the isotopic composition of the atmospheric vapour as the average value for two idealized situations: (i) locally sourced vapour which has the same isotopic composition as the sublimation flux; (ii) non-locally sourced vapour in isotopic equilibrium with snowfall. Model Sublimation is run with a time step of 1 h, independently of Model Air Parcel.

 Model Air Parcel
Every hour, an ensemble of trajectories arrives at different heights in the ABL above the ship. For each of these trajectories, we consider an air parcel with a constant volume of 1 x 1 x 1 m3. The air parcels are initialized at the first suitable time when the trajectories are located in the ABL, either over the ice-free ocean in conditions of evaporation or over snow (Antarctic Ice Sheet or sea ice). Subsequently, the masses of the water isotopologues in the air parcels are simulated with a time step of 3 h, considering vapour uptake or removal due to the moisture flux at the snow or liquid ocean surface (only if the parcel is in the ABL) and cloud/precipitation formation (if the saturation specific humidity is reached). Sea ice is taken into account in a very simplified way. We represent the sea ice by grid cells with a sea-ice cover of more than 90% and assume the isotopic composition of the sublimation flux to be identical to that in the nearest grid cell of the Antarctic Ice Sheet. The isotopic composition of the sublimation flux is taken from Model Sublimation whereas the isotopic composition of the vapour deposition flux (over snow) and condensation flux (over ice-free ocean) is simulated assuming an isotopic equilibrium with the air parcel. Isotope effects of cloud/precipitation formation are represented using the classic Rayleigh distillation model with equilibrium fractionation, where the cloud water is assumed to precipitate immediately after formation.

 References

Hersbach, H., Bell, B., Berrisford, P., Biavati, G., Horanyi, A., Munoz Sabater, J.,... others (2018). *ERA5 hourly data on single levels from 1979 to present. Copernicus Climate Change Service (C3S) Climate Data Store (CDS)*. doi: 10.24381/cds.bd0915c6

Thurnherr, I., Wernli, H., & Aemisegger, F. (2020a). *10-day backward trajectories from ECMWF analysis data along the ship track of the Antarctic Circumnavigation Expedition in austral summer 2016/2017*. Zenodo. doi: 10.5281/zenodo.4031705

backward-trajectories

display_name: backward-trajectories

evaporation

display_name: evaporation

isotopic-distillation

display_name: isotopic-distillation

lagrangian-analysis

display_name: lagrangian-analysis

snow-sublimation

display_name: snow-sublimation

stable-water-isotopes

display_name: stable-water-isotopes

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: Modeled Isotopic Composition of Water Vapour Along Air Parcel Trajectories in the Antarctic


maintainer: Matthias Haeni

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

state: active

type: dataset

en: Field station data (OTF)

media_type: text/csv

en: Data file.

format: CSV

mimetype: text/csv

en: Data plot of the forest station (OTB)

media_type: application/pdf

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

format: PDF

mimetype: application/pdf

en: Site photo of the field station (OTF)

en: Site photo of the field station from below (viewing upwards the slope).

format: SERVICE

mimetype: image/jpeg

en: Site aerial photo (Othmarsingen)

en: Site aerial photo from both Othmarsingen stations. Source: Google. 2016. Site aerial photo from both Othmarsingen stations. Retrieved November 11, 2016, from https://www.google.ch/maps

en: Forest station data (OTB)

en: Site photo of the forest station (OTB)

en: Site photo of the forest station from above (viewing downwards the slope).

en: Data plot of the field station (OTF)

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 two meteorological stations in Othmarsingen in Switzerland where one station is located within a natural deciduous forest stand (OTB) with European beech (_Fagus sylvatica_; 120-140 yrs) and lime trees (_Tilia sp._; 120-140 yrs) as dominant tree species. A second station is situated in the very vicinity outside of the forest (field station, OTF). The meteorological time series are presented in hourly time resolution of air temperature, relative humidity, precipitation, photosynthetically active radiation (PAR) and wind speed. Othmarsingen 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

educ

fr: Éducation, culture et sport

de: Bildung, Kultur und Sport

it: Istruzione, cultura e sport

fr: EnviDat: le portail de données environnementales

de: EnviDat: das Umwelt-Datenportal

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.

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: Othmarsingen, Switzerland: Long-term forest meteorological data from the Long-term Forest Ecosystem Research Programme (LWF), from 1996 onwards


en: glaciers conservation extreme-habitat arctic fungi bacteria active-layer permafrost biodiversity plastisphere swiss-alps biobank collections

en: Complete collection of bacterial and fungal isolates from Permafrost, active layer and glaciers in Switzerland, Svalbard, northern Greenland and Russia.

format: XLS

en:
The cold habitats of the Swiss Alps and the Arctic are undergoing change and are at risk of disappearing completely or partially in the future. Along with them, a poorly known diversity of microorganisms that have adapted to life in these supposedly hostile places. By cryopreserving microorganisms from these habitats, some of today's biodiversity can be preserved in biobanks.
The collection contains cryopreserved bacteria and fungi isolated from permafrost and active layer of Muot da Barba Peider and Val Lavirun, from the glacier forefield and glacier toe of the Damma glacier, from active layer in northern Greenland and from plastic waste in Svalbard, as well as isolates from plastic incubations in Muot da Barba Peider, northern Greenland and arctic Russian soils.
Project overview: https://www.wsl.ch/en/projects/life-at-chilly-temperatures-a-collection-of-microorganisms-from-extreme-habitats/

active-layer

display_name: active-layer

arctic

display_name: arctic

bacteria

display_name: bacteria

biobank

display_name: biobank

biodiversity

display_name: biodiversity

collections

display_name: collections

conservation

display_name: conservation

extreme-habitat

display_name: extreme-habitat

fungi

display_name: fungi

glaciers

display_name: glaciers

permafrost

display_name: permafrost

plastisphere

display_name: plastisphere

swiss-alps

display_name: swiss-alps

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: Life at chilly temperatures - A collection of microorganisms from extreme habitats


en: grayzone wrf cosmo-wrf numerical-simulation complex-terrain

media_type: application/zip

format: ZIP

en:
This dataset contains simulation data for *"Influence of Air Flow Features on Alpine Wind Energy Potential" (Kristianti et al., 2024).*
•	The WRF_dia2702 and WRF_dia1103 folders contain the namelist.wps, namelist.input, and output files from the simulation in the Diablerets region on 27/02/2021 and 11/03/2021, respectively.
•	The WRF_luk2310 and WRF_luk0912 folders contain the namelist.wps, namelist.input, and output files from the simulation in the Lukmanier region on 23/10/2020 and 09/12/2020, respectively.
•	The postprocessing file contains Python codes used to create figures in Kristianti et al. (2024).
**Notes:**
•	Topography input is provided by Gerber et al. (2021).
•	Simulations are run using the COSMO-WRF model developed by Gerber et al. (2018).
•	Visualization by Python code uses wrf-python provided by Ladwig et al. (2017).
*This dataset was produced by the EDGE consortium sponsored by the Swiss Federal Office of Energy's SWEET programme, Swiss National Science Foundation (SNSF): Grant 179130, and the Swiss National Supercomputing Centre (CSCS) projects s938, s1115 and s1242.*

complex-terrain

display_name: complex-terrain

cosmo-wrf

display_name: cosmo-wrf

grayzone

display_name: grayzone

numerical-simulation

display_name: numerical-simulation

wrf

display_name: wrf

en: COSMO-WRF Dataset for Swiss Alps Simulations in Gray-Zone Resolution


mountain-permafrost-hydrology

maintainer: Jeannette Noetzli

title_for_slug: mountain-permafrost-hydrology

en: monitoring-techniques mountain-permafrost-hydrology climate-change-impacts mass-movements permafrost-degradation ice-rich-permafrost

en: Synthesis report chapter of the Hydro-CH2018 project of the Federal Office for the Environment (FOEN)

en: DORA Persistent URL

en: This report was prepared as one of the synthesis report chapters of the Hydro-CH2018 project of the Federal Office for the Environment (FOEN). In earlier reports such as the CH2014-IMPACTS report (CH-Impacts 2014), the topic of mountain permafrost hydrology was not addressed. Here, we provide a baseline of the available knowledge of mountain permafrost in the Swiss Alps for future reference. We compile an overview of the current understanding of mountain permafrost in the Swiss Alps, its distribution and characteristics, observed and projected changes, and expected impacts on slope stability, infrastructure and hydrological aspects. We also briefly describe the measurement techniques and modelling approaches applied. The chapter closes with a summary of the most important open research questions. The literature cited mainly includes studies on mountain permafrost published in scientific journals and assessments of long-term observation data. We focus on permafrost hydrology interactions wherever information is available. However, systematic studies on permafrost hydrology in mountain areas are still limited.

climate-change-impacts

display_name: climate-change-impacts

ice-rich-permafrost

display_name: ice-rich-permafrost

mass-movements

display_name: mass-movements

monitoring-techniques

display_name: monitoring-techniques

mountain-permafrost-hydrology

display_name: mountain-permafrost-hydrology

permafrost-degradation

display_name: permafrost-degradation

en: Mountain Permafrost Hydrology


maintainer: Anita Risch

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

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- 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-functions

display_name: ecosystem-functions

ecosystem-multifunctionality

display_name: ecosystem-multifunctionality

exclusion

display_name: exclusion

grassland

display_name: grassland

grazing

display_name: grazing

invertebrates

display_name: invertebrates

subalpine

display_name: subalpine

swiss-national-park

display_name: swiss-national-park

vertebrates

display_name: vertebrates

en: Ecosystem coupling and multifunctionality - exclosure experiment


maintainer: Frank Techel

en: avalanche-size avalanche machine-learning natural-avalanches snowpack-model

en: Data set DL was used for validation of the avalanche-day classifier and the avalanche-size estimator. The data set contains the quality-checked danger levels merged with the respective SNOWPACK simulations (Sections 2.3 and 3.3(2) in Mayer et al.).

en: Data set AV1 was used for training the avalanche-day classifier (Sections 2.1.1, 2.2, and 3.1 in Mayer et al.).

en: Data set AV2 used for training the avalanche-size estimator (Sections 2.1.2 and 3.2 in Mayer et al.)

en: Data set AV3 was used for validation of the avalanche-day classifier (Sections 2.1.3 and 3.3(1) in Mayer et al.).

en:
The data set contained in this repository was used in the analysis by Mayer et al. (2023):
Mayer, S. I., Techel, F., Schweizer, J., and van Herwijnen, A.: Prediction of natural dry-snow avalanche activity using physics-based snowpack simulations, EGUsphere, https://doi.org/10.5194/egusphere-2023-646, 2023.

avalanche

display_name: avalanche

avalanche-size

display_name: avalanche-size

machine-learning

display_name: machine-learning

natural-avalanches

display_name: natural-avalanches

snowpack-model

display_name: snowpack-model

educ

en: Education, culture and sport

en: Data-set for prediction of natural dry-snow avalanche activity and avalanche size using physics-based snowpack simulations


en: chondrichthyes dna-metabarcoding atlantic-region fish-composition edna teleo actinopterygii bay-biscay

en: Data access

en:
Environmental DNA complements scientific trawling in surveys of marine fish biodiversity (Dataset 2020)

In October 2020 we chose 16 sites from the 2020 EVHOE survey for eDNA sampling. The French international EVHOE bottom trawl survey is carried out annually during autumn in the BoB to monitor demersal fish resources. All sites were located on the continental shelf (26–170 m depth), except one on the upper slope with a depth of 1045 m. To perform eDNA sampling, we collected water samples at 15 sites (Figure 1a). At each site, we sampled seawater using Niskin bottles deployed with a circular rosette. There were nine bottles on the rosette, each of them able to hold ∼5 l of water. At each site, we first cleaned the circular rosette and bottles with freshwater, then lowered the rosette (with bottles open) to 5 m above the sea bottom, and finally closed the bottles remotely from the boat. The 45 l of sampled water was transferred to four disposable and sterilized plastic bags of 11.25 l each to perform the filtration on-board in a laboratory dedicated to the processing of eDNA samples. To speed up the filtration process, we used two identical filtration devices, each composed of an Athena® peristaltic pump (Proactive Environmental Products LLC, Bradenton, Florida, USA; nominal flow of 1.0 l min–1 ), a VigiDNA 0.20 μm filtration capsule (SPYGEN, le Bourget du Lac, France), and disposable sterile tubing. Each filtration device filtered the water contained in two plastic bags (22.5 l), which represent two replicates per sampling site. We followed a rigorous protocol to avoid contamination during fieldwork, using disposable gloves and single-use filtration equipment and plastic bags to process each water sample. At the end of each filtration, we emptied the water inside the capsule that we replaced by 80 ml of CL1 conservation buffer and stored the samples at room temperature following the specifications of the manufacturer (SPYGEN, Le Bourget du Lac, France). We processed the eDNA capsules at SPYGEN, following the protocol proposed by Polanco-Fernández et al., (2020). We performed library preparation and sequencing at Fasteris (Geneva, Switzerland). Specifically, we prepared four libraries using the MetaFast protocol (a ligation-based method) and sequenced them separately. We carried out paired-end sequencing using a MiSeq sequencer (2 × 125 bp, Illumina, San Diego, CA, USA) on two MiSeq Flow Cell Kits (v3; Illumina), following the manufacturer’s instructions. We analysed the sequence reads using the OBITools package (http:
//metabarcoding.org/obitools; Boyer et al., 2016), following the protocol described by Valentini et al. (2016).

Data content:
	* rawdata/: contains the raw reads for each individual sample. One archive contains the paired-end reads specified by the _R1 or _R2 suffix as well as individually tagged PCR replicates (if available) together with an archive containing all extraction and PCR blank samples of the library. Reads have been demultiplexed using cutadapt but not trimmed, individual demultiplexing tags and primers remain present in the sequences.
	* taxadata/: contains the table with all detected taxonomy for each sample after bioinformatic processing (see Polanco et al. 2020 for details; https://doi.org/10.1002/edn3.140) and associated field metadata.
	* metadata/: contains two metadata files, one related to the data collected in the field for each filter, and the second related to the sequencing process in the lab (including the tag sequence, library name, and marker information for each sample)

actinopterygii

display_name: actinopterygii

atlantic-region

display_name: atlantic-region

bay-biscay

display_name: bay-biscay

chondrichthyes

display_name: chondrichthyes

dna-metabarcoding

display_name: dna-metabarcoding

edna

display_name: edna

fish-composition

display_name: fish-composition

teleo

display_name: teleo

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: Environmental DNA Marine France Evhoe 2020


en: datensatz wasserkraft schweiz speed2zero kleinstwasserkraftwerke

en: Shapefile der Einzugsgebiete (2 km² ), in denen sich die jeweiligen Kleinstwasserkraftwerke befinden (erstellt von Yasser Haddad. ETH).

en: Shapefile der 2’388 registrierten Wasserkraftanlagen in der Schweiz aus den beiden Datensätzen WASTA (> 300 kW) und CH-Kleinstwasserkraftwerke (≤ 300 kW).

en: .XLSX-Datei von CH-Kleinstwasserkraftwerke: 1'682 Kleinstwasserkraftwerke (≤ 300 kW) in der Schweiz.

en: .XLSX-Datei der 2’388 registrierten Wasserkraftanlagen in der Schweiz aus den beiden Datensätzen WASTA (> 300 kW) und CH-Kleinstwasserkraftwerke (≤ 300 kW).

en: Shapefile von CH-Kleinstwasserkraftwerke: 1'682 Kleinstwasserkraftwerke (≤ 300 kW) in der Schweiz.

en: Die 1'682 erfassten Kleinstwasserkraftwerke im Datensatz CH-Kleinstwasserkraftwerke

en:
In der Schweiz werden Wasserkraftanlagen (WKA) mit einer Leistung von mehr als 300 kW systematisch erfasst und in der nationalen Wasserkraftstatistik (WASTA) zusammengetragen. Die WASTA bildet eine umfangreiche Datengrundlage für Analysen bezüglich Wasserkraft, auch im Kontext von Klimawandel, Biodiversitätsverlust und Energiewende. Nicht erfasst auf nationaler Ebene waren bis anhin die sogenannten Kleinstwasserkraftwerke, WKA mit einer Leistung von weniger als 300 kW. Kleinstwasserkraftwerke tragen zwar nicht wesentlich zur Schweizer Elektrizitätsversorgung bei, haben jedoch aufgrund ihrer hohen Anzahl Auswirkungen auf die Gewässerökologie, die mit den Klimawandel noch stärker unter Druck gerät.
Der neu erstellte Datensatz CH-Kleinstwasserkraftwerke umfasst 1'682 WKA mit einer Leistung von weniger als 300 kW. In den zwei Datensätzen WASTA (> 300 kW) und CH-Kleinstwasserkraftwerke (≤ 300 kW) sind zurzeit 2’388 WKA erfasst. Im Austausch mit den 26 Kantonen wurde jedoch klar, dass es sich nicht um eine vollständige Sammlung von Kleinstwasserkraftwerken handelt. Die 1'682 Kleinstwasserkraftwerke machen rund 70% aller erfassten WKA in der Schweiz aus, tragen jedoch mit weniger als 600 GWh/Jahr lediglich rund 1.5% zur schweizerischen Wasserkraftproduktion bei. In einem optimistischen Szenario, in dem die jährliche Produktionserwartung tendenziell überschätzt wird, liegt dieser Anteil um 0.3% höher. Von den erfassten 2’388 WKA erzeugen die 10% der grössten Anlagen über 90% der schweizerischen Wasserkraftproduktion. Der Datensatz CH-Kleinstwasserkraftwerke ist im Rahmen der ETH-Initiative SPEED2ZERO entstanden, die Klimadienstleistungen in den Bereichen Klimawandel, Biodiversitätsverlust und Energiewende erbringt (https://speed2zero.ethz.ch).
Hier verfügbare Datensätze:
- CH-Kleinstwasserkraftwerke - der hier vorgestellte Datensatz mit 1'682 Kleinstwasserkraftwerken
- EZG-Kleinstwasserkraftwerke - die Einzugsgebiete (2 km² ), in denen sich die 1'682 Kleinstwasserkraftwerke befinden (erstellt von Yasser Haddad. ETH)
- Metadaten - sämtliche Metadaten zum Datensatz CH-Kleinstwasserkraftwerke
- CH-WKA - eine Zusammenstellung sämtlicher 2'388 erfassten Wasserkraftanlagen in der Schweiz aus den beiden Datensätzen WASTA (> 300 kW) und CH-Kleinstwasserkraftwerke (≤ 300 kW)

datensatz

display_name: datensatz

kleinstwasserkraftwerke

display_name: kleinstwasserkraftwerke

schweiz

display_name: schweiz

wasserkraft

display_name: wasserkraft

en: CH-Kleinstwasserkraftwerke - ein schweizweiter Datensatz zu Kleinstwasserkraftwerken


maintainer: EnviDat Support

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

en: Site aerial photo (Neunkirch)

en: Site aerial photo from both Neunkirch stations. Source: Google. 2016. Site aerial photo from both Neunkirch stations. Retrieved November 11, 2016, from https://www.google.ch/maps

en: Site photo of the forest station (NEB)

en: Site photo of the forest station from below (viewing upwards the slope).

en: Field station data (NEF)

en: Data file.

en: Data plot of the field station (NEF)

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

en: Data plot of the forest station (NEB)

en: Site photo of the field station (NEF)

en: Site photo of the field station from the side.

en: Forest station data (NEB)

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 two meteorological stations in Neunkirch in Switzerland where one station is located within a natural deciduous forest stand (NEB) with European beech (_Fagus sylvatica_; 160 yrs), sycamore maple (_Acer pseudoplatanus_; 160 yrs) and lime trees (_Tilia sp._; 110 yrs) as dominant tree species. A second station is situated in the very vicinity outside of the forest (field station, NEF). The meteorological time series are presented in hourly time resolution of air temperature, relative humidity, precipitation, photosynthetically active radiation (PAR) and wind speed. Neunkirch 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

educ

en: Education, culture and sport

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


en: backward-trajectories raclets clouds ice-nucleation aerosol

en: This dataset contains number concentrations of ice-nucleating particles active at -15 °C observed at Weissfluhjoch during February and March 2019, as well as complementary data (measured aerosol number concentrations and modelled total precipitation along air mass trajectories). This data formed the basis of our paper with the title “Towards parameterising atmospheric concentrations of ice-nucleating particles active at moderate supercooling”.

aerosol

display_name: aerosol

backward-trajectories

display_name: backward-trajectories

clouds

display_name: clouds

ice-nucleation

display_name: ice-nucleation

raclets

display_name: raclets

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: Ice nucleating particle concentrations active at -15 °C at Weissfluhjoch


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

en: Site photo of the forest station (BTB)

en: Site photo of the forest station from the side.

en: Site photo of the field station (BTF)

en: Data plot of the forest station (BTB)

en: Field station data (BTF)

en: Data plot of the field station (BTF)

en: Site aerial photo (Bettlachstock)

en: Site aerial photo from both Bettlachstock stations. Source: Google. 2016. Site aerial photo from both Bettlachstock stations. Retrieved November 11, 2016, from https://www.google.ch/maps

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 two meteorological stations in Bettlachstock in Switzerland where one station is located within a natural mixed forest stand (BTB) with European beech (_Fagus sylvatica_; 170-190 yrs), European silver fir (_Abies alba_; 190 yrs) and Norway spruce (_Picea abies_; 200 yrs) as dominant tree species. A second station is situated in the very vicinity outside of the forest (field station, BTF). The meteorological time series are presented in hourly time resolution of air temperature, relative humidity, precipitation, photosynthetically active radiation (PAR) and wind speed. Bettlachstock is part of the Long-term Forest Ecosystem Research Programme (LWF) established and maintained by the Swiss Federal Research Institute WSL.

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


maintainer: Anita C. Risch

en: global nutrient-network mineralization soil-biology grassland soil worldwide soil-chemistry

en:
site.code: Site code

Continent: Continent

sampleID: Sample ID

nn.latitude: Lattitude

nn.longitude: Longitude

bioclim.T.ann: Mean annual temperature (°C)

bioclim.T.var: Temperature variability (°C)

bioclim.T.q.wet: Temperature of the wettest quarter (°C)

bioclim.T.q.dry: Temperature of the driest quarter (°C)

bioclim.T.q.warm: Temperature of the warmest quarter (°C)

bioclim.P.ann: Mean annual preciptiation (mm)

bioclim.P.q.wet: Precipitation of the wettest quarter (mm)

ch.pH: pH

ch.WSK.vol: Water holding capacity (vol%)

ch.bulkdensity.gcm3: Bulk density (g cm-3)

ch.porespace: Pore space (vol%)

ch.sand.perc: Soil texture: sand (%)

ch.silt.perc: Soil texture: silt (%)

ch.clay.perc: Soil texture: clay (%)

ch.NO3start.mgg: NO3 at the beginning of the incubation (mgkg)

ch.Ntot.perc: Total soil N (%)

ch.Ctot.perc: Total soil C (%)

ch.Corg.perc: Soil organic C (%)

ch.netNminfield.mgkgd: Realised soil net N mineralisation (mg kg-1 d-1)

ch.netNminlab.mgkgd: Potential soil ne N mineralisation (mg kg-1 d-1)

archaea.cpg.log: Ammonia oxidising archaea (archaeal amoA gene copies g-1 soil)

bacteria.cpg.log: Ammonia oxidising bacteria (bacterial amoA gene copies g-1 soil)

micr.biom: Microbial biomass (ug g-1 soil)

ch.CtoN: C to N ratio

ch.netNnitriffield.mgkgd.sqrt: Realised soil net nitrification, transformed (mg kg-1 d-1)

ch.netNammoniffield.mgkgd.sqrt: Realised soil net ammonification, transformed (mg kg-1 d-1)

ch.netNnitriflab.mgkgd.sqrt: Potential soil net nitrification, transformed (mg kg-1 d-1)

ch.netNammoniflab.mgkgd.sqrt: Potential soil net ammonifiation, transformed (mg kg-1 d-1)

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

Paper Citation:

Risch, A. C.; Zimmermann, S.; Ochoa-Hueso, R.; Schütz, M.; Frey, B.; Firn, J. L.; Fay, P. A.; Hagedorn, F.; Borer, E. T.; Seabloom, E. W.; et al. Soil net nitrogen mineralisation across global grasslands. Nat. Commun. 2019, 10 (1), 4981 (10 pp.). doi.org/10.1038/s41467-019-12948-2

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

We conducted coordinated measurements of realised and potential soil net Nmin, and assessed water holding capacity, bulk density, C and N content, texture, pH, pore space, microbial biomass, and archaeal (AOA) and bacterial (AOB) ammonia oxidiser abundance using identical materials and methods across 30 grasslands on six continents. The sites covered a globally relevant range of climatic and edaphic conditions. Climate data was obtained from worldclim - Global climate data https://www.worldclim.org/

global

display_name: global

grassland

display_name: grassland

mineralization

display_name: mineralization

nutrient-network

display_name: nutrient-network

soil

display_name: soil

soil-biology

display_name: soil-biology

soil-chemistry

display_name: soil-chemistry

worldwide

display_name: worldwide

educ

en: Education, culture and sport


maintainer: Marco Moretti

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

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: Response and predictors used for the SEMs

en: Metadata for the predictors and response dataset

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: Metadata for the predictor and response dataset

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: 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: Niche partitioning between wild bees and honeybees


maintainer: Virginie Marques

en: marine environmental-dna biodiversity fish plankton fjord dna-metabarcoding

en: Metabarcoding data

en: Raw metabarcoding data for both primers (teleo and 18S) and corresponding file to perform the demultiplexing and primer trimming

en: Code, data and figures

en: Here there are all the data and code to reproduce the figures and analysis presented in the paper, with a README.md file

en:
This dataset contains the raw environmental DNA data associated with the publication *Environmental drivers of eukaryotic plankton and fish biodiversity in an Arctic fjord* in the journal Polar Biology (2023).

 Methods

**Sampling**
We sampled the Lilliehöök fjord on the west coast of Spitsbergen (Svalbard, Norway) over 3 days from 3 to 5 of August 2021. Samples were taken from the glacier front up to the fjord mouth of the Krossfjorden system, around 30 km long, after the Lilliehöök fjord merged with the mouth of Möller fjord. The fjord’s maximum depth has been recorded at 373 m (Svendsen et al. 2002) and has no sill at its entrance, thereby facilitating water exchange with the open ocean of the West Spitsbergen Current. We used a research vessel to sample 5 sites for a total of 15 samples, sampling 3 depths per site (3-m, chlorophyll a maximum and 85-m, unless sea floor was shallower). Shallow and intermediate samples between 3-m and 12-m represent ~35-L of water filtered in-situ using long tubing and a peristaltic pump, and all other deeper samples were taken from a total of 3 Niskin bottles (General Oceanics), representing 22-L of water sampled per sample. Water was filtered through a VigiDNA filtration capsule (SPYGEN) with a 0.20-µm pore size using an Athena peristaltic pump (Proactive Environmental Products, Bradenton, Florida) with a flow rate of ~1-L/min. Each sample was handled with single use tubing and gloves.

**Molecular**
To perform the amplification, we used two sets of primers: teleo (forward: ACACCGCCCGTCACTCT, reverse: CTTCCGGTACACTTACCATG; Valentini et al. 2016) and the universal eukaryotic 1389F/1510R primer pair, amplifying the V9-18S rDNA gene (Amaral-Zettler et al. 2009) (forward: TTGTACACACCGCCC, reverse: CCTTCYGCAGGTTCACCTAC).

 Data content:

+ Metabarcoding data: This zip file contains the 2 sequencing libraries filtered to only retain the samples used in the present study.
+ Code, data and figure: This zip file contains all data and code to reproduce the figures and the analysis in the study, with an associated README explaining the content of each folder.

 Additional informations
For more details, please see the Methods in the associated publication: DOI: 10.1007/s00300-023-03187-9.

biodiversity

display_name: biodiversity

dna-metabarcoding

display_name: dna-metabarcoding

environmental-dna

display_name: environmental-dna

fish

display_name: fish

fjord

display_name: fjord

marine

display_name: marine

plankton

display_name: plankton

en: Data: Environmental drivers of eukaryotic plankton and fish biodiversity in an Arctic fjord


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

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

en: A condensed instruction for running the presented simulations.

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

educ

en: Education, culture and sport

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


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

en: Snowmicroquakes Data

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

en: README

media_type: text/plain

en: README file explaining the organization of the data

format: TXT

en:
When snow is compressed with a certain speed, micro-snowquakes are triggered in the porous structure of bonded crystals. The present dataset covers uniaxial compression experiments of snow at different strain rates and concurrent X-ray tomography imaging documenting this feature.

The experiments were conducted in a micro-compression stage operated in the X-ray tomography scanner in the SLF cold laboratory. The dataset comprises the compression force data of 17 compression experiments, the 3D image data from 4 X-ray tomography scans and the results of numerical simulations.

compression-experiments

display_name: compression-experiments

microstructure

display_name: microstructure

snow

display_name: snow

snow-mechanics

display_name: snow-mechanics

x-ray-tomography

display_name: x-ray-tomography

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: Compressive stick slip and snow-micro-quakes


maintainer: Tobias Wechsler

en: decision-making ecosystem-protection integral-water-management gis hydropower

en: Indicators

en: The indicators capture supporting ecosystem functions.

format: SHP

en:
 A spatial dataset and tool to simultaneously assess hydropower potential and ecological potential of the Swiss river network (Version 2016)

 Introduction
The steadily growing demand for energy and the simultaneous pursuit of decarbonisation are increasing interest in the expansion of renewable energies worldwide. In Switzerland, various funding projects have been launched to promote technologies in the field of renewable energies and their application as quickly as possible. With the introduction of a funding instrument in 2009, the number of projects submitted to produce renewable energies increased rapidly. The applications for small hydropower plants (≤ 10 MW) were correspondingly numerous. However, the assessment of the environmental impact and its comparison with hydropower importance is still not standardized.
To provide a basis for decision-making, a methodology was developed to determine the overall hydropower potential of a region. A detailed assessment of each river reach, and the systematic and holistic assessment of small hydropower projects at a regional scale are combined here. The assessment of a river reach is conducted at the river space (i.e., the river and adjacent areas) and at the surrounding landscape level. The HYDROpot_integral methodology was developed as part of Carol Hemund's dissertation (2012) at the University of Bern. It allows the evaluation of river reaches holistically, regarding ecological, social, economic and cultural criteria. As a second part of the overall project, the theoretical hydropower (or hydraulic) potential was calculated for the entire river network, which complemnets the spatial assessment. In particular, it is possible to classify river reaches into those that are more suitable for hydropower production (=”use”) and those that are more suitable for protection.

 Material and method
The HYDROpot_Integral method was developed and tested on the basis of cantonal and national data (Hirschi et al. 2013). The method relies on 73 geodata sets. This holistic assessment is the key element of the entire assessment procedure. Its aim is to quantify the importance of the ecosystem functions in terms of services. The river network (GWN07) is divided into reaches of about 450m and for each reach two study units are defined. The river space (RS) records the ecosystem functions of the water body and the nearby riparian area. The length of the RS is 315 m on average in Switzerland and a maximum of 450 m, whereas the width is based on the FOEN definition (BWG 2001: 18f) and varies between 7-107 m. The surrounding landscape (SLS) is the second survey unit that records the ecosystem functions of the surrounding area over a range of 21 m to 321 m. The SLS is calculated over three times the RS width. The length of the SLS is identical to the length of the RS. The ecosystem functions are divided into three types: regulating (service A), cultural (service B) and provisioning (service C) functions. Accordingly, the assessment of the functions is divided into three parts and three values are assigned to each river reach. The more functions there are and the greater their performance, the higher these values are and the more important the corresponding functions are. Hence, these values quantify the importance of the ecosystem functions and the ecological, cultural and economic ecosystem services of each river reach. The concatenation of ecosystem services results in a value (ABC) that can occur in 125 different versions due to the chosen five-level value scale; i.e. each digit of the three-digit number sequence can be assigned a value between 1 and 5. Each of the 125 combinations, and thus each river reach, has its own characteristics determined by the assessments of the three function types. To record the suitability, the combinations are ranked according to their ecological, cultural and economic ecosystem services. These rules mean that the combination that is most suitable for hydropower production at minimum cost in terms of ecological and cultural ecosystem services and has a high economic potential is ranked first; rank 125 indicates the highest ecological and cultural ecosystem services and the lowest economic services and is therefore most suitable for protection. A river reach that is excluded from hydropower use due to legislation, a so-called priority reach, is given rank 126 from the outset and specially marked. A more detailed description of the methods can be found in Hirschi et al. 2013 [Link]. The dataset presented here presents the latest state of the HYDROpot_integral methodology applied at the national level. Only national data that is easily accessible was used in the preparation of the dataset. The cantonal data, such as renaturation and revitalization, would have to be requested by each canton individually and was excluded here. The nationwide value synthesis was made with R.
A list of data sources can be found here [link to text file]
A list of all parameters can be downloaded here [link to PDF and text files]

 Dataset description
Data is presented as a single shapefile. It contains the river network and all assessment results obtained with HYDROpot_Integral.

 Changes in the methodology compared to the original method (Hirschi et. al 2013)

 * RS_A11 Ecomorphology: recorded for the whole of Switzerland and zero values equated with NA;
individual cantons such as Zug and St. Gallen have no mapped values according to the modular
concept of the federal government, Valais and Graubünden only the main valleys, Ticino and Fribourg not
completely (BAFU 2009).
 * RS_A14 Renaturation and revitalization data: not centrally available at the time of data collection.
centrally available, therefore values in GR were equated with NA.
 * RS_A15 Dilution ratio at wastewater treatment plants (WWTPs) for discharges: Zero values
equal to NA.
 * RS_A20 Water flow: use WASTA (2013) with hydroelectric power plants (> 300 kW) under
Federal control and dams serving hydroelectricity (Dam, as of 2013).
 * RS_C05 Synoptic hazard maps: are cantonally managed at the time of data collection,
Values in GR are marked with a 5 so that the systematics in the decision tree is not affected.
is affected.
 * Water quality (RS_A15, RS_A16, RS_A17, RS_A18, RS_A19): for the evaluation of the function type.
A Nature, it is important whether the median of the five values is less than or equal to 3 in total. This
evaluation is based on the decision tree for evaluating GR (Hirschi et al. 2013:22).
Therefore, an evaluation of the station data is made where critical and possible river segments
with poor quality (median less than 3) exist. Only two longer and one short
sections in Switzerland receive a lower median than 3 for water quality.
 * SLS_B06 Visibility: For 99 percent of the river segments (30,733 of 31,062) in the canton of
Bern (2015 reduced version), the landscape area is considered to be visible. Due to this high number
of sections, a large number of viewpoints in the layer of Swisstopo and
the computation time and computability in ArcGIS, the landscape area is classified as generally viewable
(equal to 1).
16 Method
Additional indicators were added (see Appendix B.2):
 * SLS_A21 Dissection
 * SLS_A22 Forest areas
 * SLS_B03 Hiking trails
 * SLS_B10 Residential and vacation homes
 * SLS_B11 Tourist infrastructure
 * SLS_C01 Landfill
 * SLS_C03 Infrastructure
 * SLS_C05 Industry
 * SLS_C06 Agricultural land
Not to be added, although present to some extent:
 * SLS_B06 Cultural assets of national importance: here, too, the calculability of the visibility analysis is
for the whole of Switzerland is limited
 * SLS_A15 Legally binding protection and land use planning: the individual river sections are not
clearly designated, i.e. no geodata exist
The following data are also not supplemented, as they are cantonal data:
 * SLS_A10 Cantonal nature reserves
 * SLS_A16 Forest reserves
 * SLS_A17 Cantonal inventories and contractually protected areas

decision-making

display_name: decision-making

ecosystem-protection

display_name: ecosystem-protection

gis

display_name: gis

hydropower

display_name: hydropower

integral-water-management

display_name: integral-water-management


causal-effect-of-mfoz

title_for_slug: causal-effect-of-mfoz

en: built-up-land-change the-major-function-oriented-zone causality propensity-score-matching fujian-province selection-bias

en: Data and Stata code for repeating the results

en:
Data.xlsx is the variables of 952 townships
Table 1-2 NN(1-1)_noreplace_caliper(0.01).do is STATA code to produce the results in Table 1 and 2
Figure 5 Distribution of the propensity scores.R is R code rto produce Figure 5
Figure 5 Standard mean difference.R is R code rto produce Figure 5

en:
Title: Closer to causality: How effective is spatial planning in governing built-up land expansion in Fujian Province, China?

Research objective: The Major Function Oriented Zone (MFOZ), the first strategic spatial plan in China, is developed to achieve a coordinated regional development, through spatial regulation and zoning of development. The MFOZ he MFOZ divided land into four major function-oriented zones: The development-optimized zone, the development-prioritised zone, the development-restricted zone, and the development-prohibited zone. We used propensity score marching to evaluate the effect of the MFOZ on built-up land expansion in Fujian Province over three time intervals (2013–2015, 2013–2018 and 2013–2020).

Data: Data.xlsx contains the variables of 954 towns in Fujian Province.
Town_ID is the town unique ID;
County_ID is the county unique ID;
City_ID is the city unique ID;
MFOZ is the the development-prioritised zone and the development-restricted zone (The development-optimized zone and the development-prohibited zone are excluded);
Builtup_13_15 is the built-up land expansion from 2013 to 2015;
Builtup_13_18 is the built-up land expansion from 2013 to 2018;
Builtup_13_20 is the built-up land expansion from 2013 to 2020;
Dis2water is the Euclidean distance from the town to the nearest waterbody;
Slope is the the average slope within the town;
GDP is the average GDP in 2010 within the town;
Pop is the average population in 2010 within the town;
Road is the average population in 2010 within the town;
Dis2city is the Euclidean distance from the town to the nearest prefectural city centre;
Nei_Arable, Nei_Forest, and Nei_Built.up are the area of arable land, forest land, and built-up land neighbouring town i in 2010.

Method: we used the propensity score matching to compare the changes in the amount of built-up land in the towns of the development-prioritised zone with the matched towns of the development-restricted zone. Additionally, we used three evaluation intervals (2013–2015, 2013–2018 and 2013–2020) to evaluate temporal variation in the causal effect of the MFOZ on built-up land expansion.

built-up-land-change

display_name: built-up-land-change

causality

display_name: causality

fujian-province

display_name: fujian-province

propensity-score-matching

display_name: propensity-score-matching

selection-bias

display_name: selection-bias

the-major-function-oriented-zone

display_name: the-major-function-oriented-zone

en: Causal effect of MFOZ


maintainer: Chunhong Zhao

en: urban-morphology land-dynamics austin land-use landscape

en: Land use dynamics in Austin since 1992

en: The present dataset is part of the published scientific paper Zhao C, Weng Q, Hersperger A M. Characterizing the 3-D urban morphology transformation to understand urban-form dynamics: a case study of Austin, Texas, USA. Landscape and urban planning, 2020, 203:103881. The overall objective of this paper is to understand urban form dynamics in the Austin metropolitan area for the periods 2006–2011 and 2011–2016. The study also aims to understand to what extent the changes in the built environment (in terms of ‘efficient growth’ versus ‘inefficient growth’) from the 1990s to 2016 in the Austin metropolitan area corresponded with ‘compact and efficient growth’ planning policy documents. The UMT distribution can be found in the paper. The area of transitioning UMT was provided in Table 2 and Table 3 can be found in the Appendix of the paper. A protocol was developed to perform the content analysis of the strategic plans and gather the data. The detailed list of protocol items can be found in Appendix B of the paper. This study demonstrates the advantage of applying Lidar data to characterize 3-D urban morphology type (UMT) transition and understand its dynamics, which helps develop a comprehensive understanding of the urbanization process and provides a tool for planning intentions and policies evaluation on urban development over time. The UMT maps can be found in Appendix A of the paper. The Lidar point datasets and the 30 × 30 m National Land Cover Database (NLCD) are the two main data sources of UMT mapping. Lidar datasets were gathered from different projects that had been conducted and collected by state agencies and other organizations between 2007 and 2017. Table A1 in the appendix in the paper shows the accuracies and acquisition parameters of the Lidar projects from 2007 to 2017. Land use/cover dynamics in Austin metropolitan area dataset provides Land use/cover patterns in the years 1992, 2001, 2004, 2006, 2008, 2011, 2013, 2016 with a spatial resolution of 30 meters. Since NLCD 1992 used a different classification system for the urban land classes, we first reclassified the NLCD 1992 using a customized Arcpy package.

austin

display_name: austin

land-dynamics

display_name: land-dynamics

land-use

display_name: land-use

landscape

display_name: landscape

urban-morphology

display_name: urban-morphology

educ

en: Education, culture and sport

en: Land use/cover dynamics in Austin metropolitan area since 1992


en: place-attachment landscape sense-of-place electrodermal-activity urban-ecology

en: 05. Visuals

en: 03. Publication Ready Data

en: 02. Questionnaire Data

en: 00. EDA Raw Data

en: 01. EDA Processed Data

en: 04. Scripts

en: This repository contains data on EDA measurements of visitors with different cultural backgrounds in virtual urban park settings. The parks are a Persian garden (Shiraz, Iran) and a historical park in Zurich, Switzerland. The cultural background of the visitors is Persian and Central European. The repository contains raw data from EDA, processed time series and statistical procedures.

electrodermal-activity

display_name: electrodermal-activity

place-attachment

display_name: place-attachment

sense-of-place

display_name: sense-of-place

urban-ecology

display_name: urban-ecology

envidat

en: EnviDat: the Environmental Data Portal

en: Electrodermal Activity (EDA) of Bi-cultural Visitors In Virtual Park Settings


en: cloud-droplets ccn hac2 aerosol hygroscopicity

en: This repository contains the datasets that were used for used for the paper:: Drivers of Droplet Formation in East Mediterranean Orographic Clouds, EGUsphere, https://doi.org/10.5194/egusphere-2024-490, 2024.

aerosol

display_name: aerosol

ccn

display_name: ccn

cloud-droplets

display_name: cloud-droplets

hygroscopicity

display_name: hygroscopicity

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: Dataset for the publication Drivers of Droplet Formation in East Mediterranean Orographic Clouds


high-resolution-climate-data-for-europe

title_for_slug: high-resolution-climate-data-for-europe

en: air-temperature eur11 europe daily-climate cordex maximum-temperature minimum-temperature precipitation

en: Data Access

en: CHELSA EUR11 Technical Documentation

en: As the CHELSA project is continuously expanded, certain new parameters, time scales etc. are not included anymore in the original publication (Karger et al. 2017). We are therefore provide this document as a guideline of the current climatic parameters available and will expand it as new parameters or time periods will become available. Please refer to the version history for changes made in the document.

en:
High-resolution information on climatic conditions is essential to many applications in environmental and ecological sciences. Here we present downscaled climate data for the CORDEX EUR11 domain at a high resolution of 30 arc sec. The temperature algorithm is based on statistical downscaling of atmospheric temperature lapse rates. The precipitation algorithm incorporates orographic predictors including wind fields, valley exposition, and boundary layer height. The resulting data consist of a daily temperature and precipitation timeseries.

The data is distributed under a: Creative Commons: Attribution 4.0 International (CC BY 4.0) license.

air-temperature

display_name: air-temperature

cordex

display_name: cordex

daily-climate

display_name: daily-climate

europe

display_name: europe

maximum-temperature

display_name: maximum-temperature

minimum-temperature

display_name: minimum-temperature

precipitation

display_name: precipitation

en: High resolution climate data for Europe