maintainer: Anita Risch

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

en: Datafile

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

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

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

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

Soil.moist	: Soil moisture (%)

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

pH: Soil pH

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

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

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

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

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

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

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

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

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

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

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

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

Plant.richness: Plant species richness

Plant.N: Plant tissue nitrogen content (%)

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

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

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

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

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

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

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

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- 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


snow-drift-station-micro-rain-radar

maintainer: EnviDat Support

title_for_slug: snow-drift-station-micro-rain-radar

en: raclets mountain snow radar precipitation rain

state: active

type: dataset

en: MMR Data Period 1

media_type: application/zip

en: The dataset contains measurements between March 1 and March 5, 2019, with time in UTC. The parameters and specifications are given in MRR_parameters.pdf. The zip folder contains hourly data files in netCDF format and a log file, reporting the instrument status.

format: ZIP

mimetype: application/zip

en: MRR data Period 2

en: The dataset contains measurements between March 5 and March 8, 2019, with time in UTC. The parameters and specifications are given in MRR_parameters.pdf. The zip folder contains hourly data files in netCDF format and a log file, reporting the instrument status.

en: MRR data of period 4

en: The dataset contains measurements between March 13 and March 22, 2019, with time in UTC. The parameters and specifications are given in MRR_parameters.pdf. The zip folder contains hourly data files in netCDF format and a log file, reporting the instrument status.

en: MRR data of period 3

en: The dataset contains measurements between March 8 and March 13, 2019, with time in UTC. The parameters and specifications are given in MRR_parameters.pdf. The zip folder contains hourly data files in netCDF format and a log file, reporting the instrument status.

en: Parameter MRR

media_type: application/pdf

en: The PDF contains additional information on parameters which were set for the certain time periods (time in UTC).

format: PDF

mimetype: application/pdf

en: The instrument (MRR, Metek) was mounted at Gotschnagrat (LON: 46.859 LAT: 9.849) at a height of 1 m above snow surface (at the beginning of the campaign) with an orientation of 22° with respect to North and a horizontal viewing direction. The sampling time was either 5 s or 10 s, depending on the settings at the specific period. The MRR produces standard outputs like radar reflectivity, doppler velocity, etc., and additional information can be found [here](https://metek.de/de/product/mrr-2/).

mountain

display_name: mountain

precipitation

display_name: precipitation

raclets

display_name: raclets

radar

display_name: radar

rain

display_name: rain

snow

display_name: snow

educ

fr: Éducation, culture et sport

de: Bildung, Kultur und Sport

en: Education, culture and sport

it: Istruzione, cultura e sport

envidat

fr: EnviDat: le portail de données environnementales

de: EnviDat: das Umwelt-Datenportal

en: EnviDat: the Environmental Data Portal

it: EnviDat: il portale dei dati ambientali

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

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

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

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

political_level: other

wsl

capacity: public

type: organization

approval_status: approved

key: guid

key: uri

value: Envidat Harvester

en: Snow Drift Station - Micro Rain Radar


maintainer: Lisa Hülsmann

en: forest-inventory fagus-sylvatica mortality-models primeval-forests tree-mortality forest-reserves

en: Swiss data reduced

media_type: text/csv

en:
READ ME for

Hülsmann L, Bugmann H, Commarmot B, Meyer P, Zimmermann S, Brang P
Data from: Does one model fit all? Patterns of beech mortality in natural forests of three European regions.
Ecological Applications http://dx.doi.org/10.5061/dryad.h4s6t

Forest inventory data of beech for the development of individual-tree mortality models from strict forests reserves in Switzerland, Germany and Ukraine.

The data package provides the files
CH_reduced: inventory data of the reduced dataset from Switzerland that was used to assess the influence of additional environmental and stand characteristics on beech mortality
CH: inventory data from strict forest reserves in Switzerland
DE: inventory data from strict forest reserves in Germany
UA: inventory data from a primeval beech forest in Ukraine

A set of three consecutive inventories was used to generate records for the calibration of mortality models based on trees that were alive in the first and second inventory and either dead or alive in the third inventory.
Diameter at breast height: dbh (mm)
Annual relative basal area increment: relBAI (), calculated based on the first and the second dbh measurement as the compound annual growth rate of the trees basal area (Bigler and Bugmann 2004)
Status of the tree: y, 0 = alive, 1 = dead
Length of the mortality period: dt (years)

Additional environmental and stand characteristics were derived for the reduced Swiss dataset.
Note the varying seasonal level of the covariates considering the entire year, the growing season from April to September (G) and the winter month January to March (W).
All climatic covariates were calculated for both the ‘growth’ (2) and the ‘mortality’ period (3). The stand covariates were derived for the second inventory of each record (2).

Mean diameter at breast height: dbh.mean.2 (mm)
Interquartile range of diameter at breast height: dbh.IQR.2 (mm)
Median diameter at breast height: dbh.median.2 (mm)
Basal area per hectare: BA.2 (m2 ha-1)
Number of trees per hectare: N.2 (ha-1)
pH-value: pH ()
Available water capacity in the soil: AWC (mm)
Mean annual precipitation sum: P.2, P.3 (mm)
Mean precipitation sum during growing season: PG.2, PG.3 (mm)
Mean annual air temperature: mT.2, mT.3 (°C)
Mean air temperature during growing season: mTG.2, mTG.3 (°C)
Mean air temperature during winter months: mTW.2, mTW.3 (°C)
Mean growing degree-days: GDD.2, GDD.3 ()
Mean number of months during growing season with water deficit: mDEFdurG.2, mDEFdurG.3 ()
Mean annual maximum water deficit: mDEFmax.2, mDEFmax.3 (mm)
Overall maximum of the annual maximum water deficit: maxDEFmax.2, maxDEFmax.3 (mm)
Mean of cumulative water deficit during growing season: mDEFcumG.2, mDEFcumG.3 (mm)
Overall maximum of cumulative water deficitduring growing season: maxDEFcumG.2, maxDEFcumG.3 (mm)
Percentage of years with at least one month water deficit: percDEF.2, percDEF.3 (%)

format: CSV

mimetype: text/csv

en: Ukrainian data

en: Swiss data full

en: German data

en:
The datasets comprise nearly 19’000 trees of European beech (_Fagus sylvatica_ L.) from unmanaged forests in Switzerland, Germany / Lower Saxony and Ukraine. Tree death was modelled as a function of size and growth, i.e., stem diameter (DBH) and relative basal area increment (relBAI). To explain the spatial and temporal variability in mortality patterns, we considered a large set of environmental and stand characteristics.

 Inventory data
The strict forest reserves in Switzerland and Germany had been established in the period of 1961-1975 and 1971-1974, respectively. Every reserve included up to 10 permanent plots ranging from 0.09 to 1.8 ha in size, with slightly irregular re-measurement intervals. Permanent plots with pure or mixed beech stands were selected from the reserves of both networks. Reserves with considerable wind disturbance during the monitored intervals were excluded from the analysis. In addition to data from the Swiss and German reserves, data from a 10 ha plot in the primeval beech forest Uholka in Western Ukraine including three remeasurements were used. The inventory data provide diameter measurements at breast height (dbh) for revisited trees with a diameter of more than 4, 7 and 6 cm for Switzerland, Germany and Ukraine, respectively.

 Mortality predictors
A set of three consecutive inventories was used to generate records for the calibration of mortality models based on trees that were alive in the first and second inventory and either dead or alive in the third inventory. As an explanatory variable, the annual relative basal area increment (relBAI) was calculated based on the first and the second dbh measurement as the compound annual growth rate of the trees basal area. Tree dbh in the second inventory was used in addition to relBAI to model tree status (alive or dead) of the third inventory.

To increase the generality of the mortality models, we selected environmental variables that are known to have a considerable influence on growth and mortality of beech. We emphasized the effects of water availability using a large set of drought characteristics that were calculated based on the local site water balance. We also related beech mortality to soil pH, temperature, precipitation and growing degree-days. Additionally, we considered stand characteristics that reflect the development stage, competition and structure of the forests.

 Further information
For further information, refer to Hülsmann _et al_. (2016) Does one model fit all? patterns of beech mortality in natural forests of three European regions. _Ecological Applications_.

fagus-sylvatica

display_name: fagus-sylvatica

forest-inventory

display_name: forest-inventory

forest-reserves

display_name: forest-reserves

mortality-models

display_name: mortality-models

primeval-forests

display_name: primeval-forests

tree-mortality

display_name: tree-mortality

en: Data from: Does one model fit all? patterns of beech mortality in natural forests of three European regions


en: afforestation mountain-forest stillberg treeline long-term-experiment

en: Dataset V1

en: This dataset is outdated and has been replaced with an updated version (see description).

format: GDB

en: Site photo

en: This site photo is outdated and has been replaced with an updated version (see description).

format: SERVICE

en: Documentation

en: This data documentation is outdated and has been replaced with an updated version (see description).

mimetype: application/msword

en:
 Important
This EnviDat entry is outdated. The most recent, usable version of the data can be found under the new EnviDat entry "Long-term afforestation experiment at the Alpine treeline site Stillberg, Switzerland." The entry can be found under this link <https://www.envidat.ch/dataset/afforestation-stillberg> and with this DOI 10.16904/envidat.397.

afforestation

display_name: afforestation

long-term-experiment

display_name: long-term-experiment

mountain-forest

display_name: mountain-forest

stillberg

display_name: stillberg

treeline

display_name: treeline

en: Long-term treeline research dataset at Stillberg, Davos


maintainer: Franziska Gerber

en: surface-mass-balance reproducibility antarctica cryowrf blowing-snow

en: Processed WRF output (run with Noah-MP land surface model) used for the analysis and the figures in the paper.

en: Processed CRYOWRF output used for the analysis and the figures in the paper.

en: Namelist and input files and information to run the WRF and CRYOWRF simulations used in the paper.

en: Static input data from the WRF simulations (used in the python scripts in Scripts_Reproducibility).

en: Python scripts to reproduces figures in Gerber et al., 2022, revised

mimetype: application/x-zip-compressed

en: Python scripts to reproduces figures in Gerber et al., 2022, submitted.

en:
This dataset contains data and scripts for "CRYOWRF - a validation and the effect of blowing snow on the Antarctic SMB" (Gerber et al., submitted).

* Simulation_setup: Namelists and input information to run the simulation. Some input files need to be downloaded from Sharma et a., 2021.
* Static_input: Static topography input file of WRF (geo_em.d01).
* WRF_27km_NoahMP: Preprocessed WRF output of the simulation run with the WRF using the surface parameterization Noah-MP to reproduce the figures and results in the paper.
* WRF_27km_CRYOWRF: Preprocessed WRF output of the simulation run with CRYOWRF to reproduce the figures and results in the paper.
* Scripts_Reproducibility: Python scripts to reproduce the figures and results in the paper.

Note:

* To run some of the scripts Atmospheric Weather station data needs to be prepared using Gerber and Lehning, 2022.
* AWS data is not provided and needs to be downloaded from the corresponding databases. Please make sure to comply with the respective terms and conditions.

antarctica

display_name: antarctica

blowing-snow

display_name: blowing-snow

cryowrf

display_name: cryowrf

reproducibility

display_name: reproducibility

surface-mass-balance

display_name: surface-mass-balance

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: Reproducibility dataset for CRYOWRF validation


en: southern-switzerland drought-stress dendroecology spei grapevine-yellows

en: Dataset 2. Ring width.

en:
Ring width measured with cellSens from slides.
Measures expressed as [μm] and arranged per ID (see dataset 1) and year.

en: Dataset 1

en: Sample identification, symptomatology (symptomatic vs. asymptomatic), coordinates (CH1903), phloem disarrangement class, drought-sensitivity, slope sector.

en:
Dataset collected from dendroecological study on trunks of grapevines ('Chardonnay' cv.) infected by the "Flavescence dorée" phytoplasma (FDp) in Origlio (southern Switzerland) in 2019-2020. Ring widths were measured with cellSens (Olympus Corporation). Calculations and analysis were conducted within R.
The Flavescence dorée phytoplasma (FDp) causes a severe grapevine (Vitis vinifera) disease. Anatomical modification due to FDp infections are known to occur but research so far focused on stems and leaf tissues and, in particular, on their phloem structure. In this paper, we applied dendrochronological techniques on wood rings and analysed the anatomical structures of the trunk of the susceptible grapevine cultivar ‘Chardonnay’ in order to verify their response to FDp infections.
In this study, we tested the impact of FDp and drought stress on xylem ring width and also described phloem anomalies inside the trunk of grapevines. We concluded that drought and FDp infection both have a significant effect on ring width reductions and that FDp supersedes the effect of drought conditions (calculated after the SPEI index) in infected specimens.

dendroecology

display_name: dendroecology

drought-stress

display_name: drought-stress

grapevine-yellows

display_name: grapevine-yellows

southern-switzerland

display_name: southern-switzerland

spei

display_name: spei

en: Impact of the “Flavescence dorée” phytoplasma on xylem growth and phloem anomalies in trunks of ‘Chardonnay’ grapevines (Vitis vinifera)


biomass-of-lying-dead-wood-lis

title_for_slug: biomass-of-lying-dead-wood-lis

en:
Dry weight (mass) of lying deadwood starting at 7 cm in diameter that does not fulfil the criteria for a tally tree (measurement location of dbh not identifiable or the dbh is less than 12cm).

Citation:
 > _Abegg, M.; Brändli, U.-B.; Cioldi, F.; Fischer, C.; Herold-Bonardi, A.; Huber M.; Keller, M.; Meile, R.; Rösler, E.; Speich, S.; Traub, B.; Vidondo, B. (2014). Fourth national forest inventory - result tables and maps on the Internet for the NFI 2009-2013 (NFI4b). [Published online 06.11.2014] Available from World Wide Web http://www.lfi.ch/resultate/ Birmensdorf, Swiss Federal Research Institute WSL. [doi:10.21258/1057112](https://doi.org/10.21258/1057112)_

accessible-forest-without-shrub-forest

display_name: accessible-forest-without-shrub-forest

biogeographical-region

display_name: biogeographical-region

biomass-of-lying-dead-wood-lis

display_name: biomass-of-lying-dead-wood-lis

canton

display_name: canton

economic-region

display_name: economic-region

ownership

display_name: ownership

production-region

display_name: production-region

protection-forest-region

display_name: protection-forest-region

en: Biomass of lying dead wood (LIS)


maintainer: Marcia Phillips

en: temperature permafrost gemsstock permos borehole

en: Map of PERMOS borehole network

en: DATASET & PLOTS

en: Data visualiser and download service provided by PERMOS.

en: PERMOS DATA POLICY

en:
Processed ground temperature measurements at the Gemsstock permafrost borehole in canton Uri, Switzerland. The borehole is located at 2940 m asl on a steep (50°) North-West slope (315°). The surface material is bedrock and borehole depth is 40 m. Thermistors used YSI 44008. Year of drilling 2006. This borehole is part of the Swiss Permafrost network, PERMOS (www.permos.ch). Contact phillips@slf.ch for details of processing applied.

Publications

1. A. Haberkorn, M. Phillips, R. Kenner, H. Rhyner, M. Bavay, S.P. Galos, M. Hoelzle. Thermal regime of rock and its relation to snow cover in steep Alpine rock walls: Gemsstock, central Swiss Alps. 2015. Geografiska Annaler: Series A, Physical Geography. Volume 97. Issue 3. 579–597. http://dx.doi.org/10.1111/geoa.12101. 10.1111/geoa.12101.

2. R. Kenner, M. Phillips, C. Danioth, C. Denier, P. Thee, A. Zgraggen. Investigation of rock and ice loss in a recently deglaciated mountain rock wall using terrestrial laser scanning: Gemsstock, Swiss Alps. 2011. Cold Regions Science and Technology. Volume 67. Issue 3. 157–164. http://dx.doi.org/10.1016/j.coldregions.2011.04.006. 10.1016/j.coldregions.2011.04.006.

borehole

display_name: borehole

gemsstock

display_name: gemsstock

permafrost

display_name: permafrost

permos

display_name: permos

temperature

display_name: temperature

en: Processed permafrost borehole data (2940 m asl), Gemsstock, Switzerland


maintainer: Merin Reji Chacko

en: environmental-dna biodiversity-assessment spatial-ecology biomonitoring dna-metabarcoding

en: Analysis and Figures

en: This zipped file includes R scripts and the datasets required to run the analyses. A README describes the columns in each dataset.

en: Genomic data

en: Fastq files, primer descriptions and the final output dataset.

en: Field Metadata

en: Information concerning the locations and times of sampling, as well as the identity of the samplers and relevant comments.

en: This dataset contains the results of a five-day field excursion which the extent to which eDNA sampling can capture the diversity of a region with highly heterogeneous habitat patches across a wide elevation gradient through multiple hydrological catchments of the Swiss Alps. Using peristaltic pumps, we filtered 60 L of water at five sites per catchment for a total volume of 1 800 L. Using an eDNA metabarcoding approach focusing on vertebrates and plants, we detected 86 vertebrate taxa spanning 41 families and 263 plant taxa spanning 79 families across ten catchments. This dataset includes two sets of data. The first (Genomic data) includes all the necessary data for the bioinformatic pipeline, whereas the second (Analysis Figures) contains tidied data and scripts for the reproduction of all figures/analyses in the article describing this study.

biodiversity-assessment

display_name: biodiversity-assessment

biomonitoring

display_name: biomonitoring

dna-metabarcoding

display_name: dna-metabarcoding

environmental-dna

display_name: environmental-dna

spatial-ecology

display_name: spatial-ecology

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: Vertebrate and plant taxa recovered from 10 catchments in Vaud using an eDNA-metabarcoding approach


en: urbanization switzerland land-use landscape-services statistical-model modeling land-use-change

en: Scripts for Assessing potential landscape service trade-offs driven by urbanization in Switzerland

en:
Scripts ordered by their main purpose within sequential folders in this ReadMe marked with

Within the folders the capital letters refer to the parallel or sequential use of the scripts; scripts here in ReadMe are marked with

 00_Function Scripts
 Functions.r
Script containing several functions for analyzing statistical models: cohen.kappa, meva.table, D2, max-Tss, plot-TSS

 Service_functions.R
Script containing functions for calculating all services and returning sums (and median for bd and rec) as well as rasters

 01_Data Preparation
 A_AS_raster_preparation.R
Preparation of the land use rasters for the years 1985, 1997, and 2009 based on the original Arealstatistik (AS/ASCH); Assigning our categories and assining new values to all "construction sites" for calibrating the models
For model projection starting point (2009) and for service calculations (all ASCH years) the "other" categories were assigned to the land use categories based on dominant neighbor, so that there were no empty cells
Creation of water & mountainous area raster that stayed stable throughout the projections
Creation of MFH raster (2009), to have as base for all new projection years, as this category never becames any other

 B_Factors_preparation.R
Preparation of the factor rasters that were used to calculate service values per cell (see Table 2): LWfactor, Transportation, Vol, Rivers, Lakes, slope, TWW, Hazard_risk

 B_Predictors_preparation.R
Preparation of the raster of the predictors used for calibrating (ASCH years) and projecting (stable) the transition models that do not depend on the land use categories: Temperature (ASCH years), solar radiation (stable), Public transportation access (stable), Elevation (stable), Workers density (ASCH years), Population change (ASCH transitions)

 B_Regions_preparation.R
Preparation of bioregions as raster to be used to mask asxxxx later to calculated services and land use area just for one region

 C_Pred_proj.R
Projecting the dynamic predictors into the future for projecting the land use transitions with the model: Linear extrapolations for workers densities and population; more detailed extrapolation of temperature (based on data for all stations that matched between the temp table we used for the calibration period and the projections from CS2M, and then making a spatial interpolation for all years based on the interpolation of temperature for all years per station)

 02_Model calibration
 A_Bioreg_pred_corr.R
Calculating correlation between the predictors for each bioregion and land use category, Output are those with too high correlation so that one predictor can be removed from transitions were both predictors occur

 A_trans_numbers_bioreg.R
Calculate transition numbers for each bioregion to decide which transitions to primarily consider

 B_Bioreg_ext_eval.R
Calculating TSS based on the external evaluation for the bioregion transitions that happened often enough to try to model them (calibration data: 85-97, evaluation data: 97-09)

 B_Bioreg_int_eval.R
Calculating TSS based on the internal evaluation for the bioregion transitions that happened often enough to try to model them (calibration data: 70%, evaluation data: 30%)

 C_Bioreg_TSS_analysis.R
Extracting TSS numbers from internal and external evaluation, calculating mean and median for each transition for each region for each evaluation method and saving as csv per region to be able to select only the transitions with high enough model performance

 D_Bioreg_Models_for_prediction.R
Calibration of the models that were then used to project land use transitions into the future; calibrated separately for each bioregion

 E_Residuals_trans_models.R
Calculation of Moran's I statistics to analyze the residuals of the land use transition models

 03_Projections
 A_Bioreg_Projections_run.R
Master script for: Extrapolaitng into the future with the regional models and then assembling for each time step to calculate new AS predictors; Several Outputs: txt file to test for NAs in Predictors, txt file with random seed number for sampling, txt file with times for calculation steps (check progress of script while running), csv sheet with projected transition frequencies, tif-rasters for every region and time step, pdf with raster plot for every region and time step

 04_Service calculation
 A_Bioreg_as_services.R
Calculate services per bioregion for years 1985, 1997, 2009

 A_Service_calculation_bioregions.R
Extracting service numbers(sums) per bioregions for all projection runs and storing them in a list of matrixes to be available for further plotting; can be run for swiss wide projections or regional ones

 05_Analysis
 A_Bioreg_ASCH_development.R
Extracting the occurrence of each category per region for all runs (first part), then for ASCH years, and then plotting them nicely; only works for regional projections

 A_Bioreg_Predictors_importanceD2.R
Calculating D2 for each transition and each considered predictor from bivariate models to get value of importance

 B_Bioreg_Pred_imp_analysis.R
Using calculated D2 to sort Predictors according to their importance for each transition

 A_Bioreg_Spatial_results_analysis.R
Plotting randomly sampled runs for ASCH and services to analyses their spatial development

 A_Bioreg_Transition_numbers_check_v1.R
Analyzing the frequency for all transitions for all regions and producing the point plots for each transition separately

 A_Bioreg_Transition_numbers_check_v2.R
Analyzing percentage and numbers of all transitions but plotting them per region and originating ASCH category

 B_Transition_Analysis.R
Further Analysis of transition numbers

 A_Service_analysis.R
Plotting of the service development for bioregions in several ways for analyzing

en: Data for Assessing potential landscape service trade-offs driven by urbanization in Switzerland

en:
The provided folder structure follows the set up of the scripts.
Data is only provided when it has been fully produced by us, otherwise dummies are given.
For data that will be produced by one of the scripts, no dummies are given.
The folders may contain sub-folders, which would be filled if the scripts were all run

 00_Analysis_Data
Data produced throughout the process of the calibration and projection that is later needed for analysis

 01_Raw_Data
Primary data from external sources that were used to compile the rasters and numbers used during the calibration and projection of landscape transitions as well as service calculation

 02_Prepared_Data
Data that will be prepared for further use by scripts are put in here
Additionally it contains the parameter sheets for the transition predictors that we compiled

 03_Model_Data
 Model outputs
Folder were the projection models statistics will be saved
 Models
Folder into which the actual transition models will be saved
 Residuals
Folder into which data on models residuals will be saved for future use

 04_Projected_Data
The output of the projections will be saved into this folder

 05_Service_Data
Any service calculations will be saved in here

 06_Results_Analysis
Any Analysis plots and tables as well as intermediate data will be saved here in the respective sub-folder

en:
Data and scripts of publication:

Madleina Gerecke, Oskar Hagen, Janine Bolliger, Anna M. Hersperger, Felix Kienast, Bronwyn Price, Loïc Pellissier (2019) Assessing potential landscape service trade-offs driven by urbanization in Switzerland. Palgrave communications.

Contains land use projections for Switzerland and scripts and data for these projections as well as the calculation of landscape services.

Data Folder:
Contains sub-folder with the data necessary for this study (provided were no copyright issues, otherwise placeholders with descriptions), and folders where produced data may be stored

Scripts Folder:
Contains scripts organized into subfolders depending on their purpose

Note: Some abbreviations within the scripts and data are derived from German words and not English.

land-use

display_name: land-use

land-use-change

display_name: land-use-change

landscape-services

display_name: landscape-services

modeling

display_name: modeling

statistical-model

display_name: statistical-model

switzerland

display_name: switzerland

urbanization

display_name: urbanization

en: Land use projections and services for Switzerland


en:
Volume of stemwood with bark of all trees and shrubs starting at 12 cm dbh that were felled between two inventories. The correction for bias with the sample Tarif trees may be so drastic that it results in negative values with small numbers of trees.

Citation:
 > _Abegg, M.; Brändli, U.-B.; Cioldi, F.; Fischer, C.; Herold-Bonardi, A.; Huber M.; Keller, M.; Meile, R.; Rösler, E.; Speich, S.; Traub, B.; Vidondo, B. (2014). Fourth national forest inventory - result tables and maps on the Internet for the NFI 2009-2013 (NFI4b). [Published online 06.11.2014] Available from World Wide Web http://www.lfi.ch/resultate/ Birmensdorf, Swiss Federal Research Institute WSL. [doi:10.21258/1057112](https://doi.org/10.21258/1057112)_

altitudinal-vegetation-zone

display_name: altitudinal-vegetation-zone

avalanches-silvaprotect

display_name: avalanches-silvaprotect

biogeographical-region

display_name: biogeographical-region

conifers-broadleaves

display_name: conifers-broadleaves

economic-region

display_name: economic-region

landslide-mudflow-silvaprotect

display_name: landslide-mudflow-silvaprotect

lower-higher-altitudinal-zones

display_name: lower-higher-altitudinal-zones

main-tree-species

display_name: main-tree-species

net-increment

display_name: net-increment

ownership

display_name: ownership

potential-cost-for-timber-harvesting

display_name: potential-cost-for-timber-harvesting

processes-in-channels-silvaprotect

display_name: processes-in-channels-silvaprotect

production-region

display_name: production-region

protection-forest-region

display_name: protection-forest-region

rockfall-silvaprotect

display_name: rockfall-silvaprotect

stage-of-stand-development

display_name: stage-of-stand-development

tree-species-woody-species

display_name: tree-species-woody-species

yield

display_name: yield

en: Yield


en: npp growth assimilation dvm forest

en: NPP anomalies

en: Spatially resolved yearly anomalies of NPP simulated by 3-PG model relative to the 1961–1990 period.

en:
Simulated net primary productivity (NPP) anomalies (percent deviation) in 1961-2018 years relative to the 1961–1990 reference period for _Picea abies_ and _Fagus sylvatica_. NPP was simulated for the species' potential distribution range in Switzerland on a 1 × 1 km grid using 3-PG model.
We first assimilated nearly 800 observation years from 271 permanent long-term forest monitoring plots across Switzerland, obtained between 1980 and 2017, into the 3-PG forest ecosystem model using Bayesian inference, reducing the bias of model predictions from.
We then estimated the NPP anomalies by first simulating the growth of _P. abies_ and _F. sylvatica_ monocultures with the average climate observed during the 1961–1990 period, until the age of 40 years (spin-up). The stands were simulated starting as 2-year-old plantations with an initial density of 10,000 trees/ha. Thinning was performed at age 20 and 35 to reach a final density of ca. 1,000 trees/ha at age 40. We then simulated 30 years forced by monthly resolved climatic data from either the 1961–1990 (reference, according to MeteoSwiss) or the 1991–2018 period. We neglected the first 40 years of simulations due to high variation in productivity caused by early stage stand development. To study the impact of climate extremes on NPP, we focused on the deviation in NPP (expressed in percentage difference from the reference period) during the 30 year period (age 41–70).

assimilation

display_name: assimilation

dvm

display_name: dvm

forest

display_name: forest

growth

display_name: growth

npp

display_name: npp

en: Net primary productivity (NPP) anomalies simulated by 3-PG model for Switzerland


en: willow pterocomma-pilosum lymantria-monacha spruce phenols cinara-pilicornis

en: Heavy metal insects

en: See ReadMe

en: In controlled model forest ecosystems young trees were exposed to heavy metals in the soil and to acid precipitation. On spruce trees Lymantria monacha caterpillars and Cinara pilicornis aphids and on willow Pterocomma pilosum aphids were reared and monitored. Developmental time and fecundity of L. monacha were recorded and in aphids colony growth was measured.

cinara-pilicornis

display_name: cinara-pilicornis

lymantria-monacha

display_name: lymantria-monacha

phenols

display_name: phenols

pterocomma-pilosum

display_name: pterocomma-pilosum

spruce

display_name: spruce

willow

display_name: willow

educ

en: Education, culture and sport

envidat

en: EnviDat: the Environmental Data Portal

en: Plant-mediated effects of heavy metals and acid rain on feeding aphids and caterpillars


title_for_slug: twig-mass-of-live-trees

en:
Dry weight (mass) of branches with a diameter under 7 cm from living trees and shrubs starting at 12cm dbh.

Citation:
 > _Abegg, M.; Brändli, U.-B.; Cioldi, F.; Fischer, C.; Herold-Bonardi, A.; Huber M.; Keller, M.; Meile, R.; Rösler, E.; Speich, S.; Traub, B.; Vidondo, B. (2014). Fourth national forest inventory - result tables and maps on the Internet for the NFI 2009-2013 (NFI4b). [Published online 06.11.2014] Available from World Wide Web http://www.lfi.ch/resultate/ Birmensdorf, Swiss Federal Research Institute WSL. [doi:10.21258/1057112](https://doi.org/10.21258/1057112)_

accessible-forest-without-shrub-forest

display_name: accessible-forest-without-shrub-forest

biogeographical-region

display_name: biogeographical-region

canton

display_name: canton

conifers-broadleaves

display_name: conifers-broadleaves

economic-region

display_name: economic-region

production-region

display_name: production-region

twig-mass-of-live-trees

display_name: twig-mass-of-live-trees

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: Twig mass of live trees


imis-measuring-network

title_for_slug: imis-measuring-network

name: WSL Institute for Snow and Avalanche Research SLF

en: snow imis automatic-weather-station new-snow measurement

en: IMIS Data Download historical data

en: For all data older than 7 days

en: IMIS data download live data

media_type: application/json

en: download live IMIS data via API

format: JSON

en: IMIS stations detailed metadata

en: Data downloadable over API and File Download

en:
The Intercantonal Measurement and Information System (IMIS) consists of nearly 200 automatic measuring stations. They are distributed throughout the Swiss Alps and the Jura region and, in most cases, are situated above the tree line, most frequently between 2000 and 3000 m. The stations record the conditions around the clock, in general every 30 minutes.
Most IMIS stations are located in the vicinity of starting zones of potentially destructive avalanches, and provide essential information to local safety officers for public safety in settlements and on the roads. They are also used for snow-hydrological and research purposes and by the avalanche warning service of the SLF.
This dataset comprises data from IMIS snow and wind stations. The snow and wind stations are usually situated close to each other and measure the key weather data required for assessing the avalanche danger.

 IMIS snow stations

Snow stations are located on wind-protected flat terrain. The snowpack model SNOWPACK calculates the layers and properties of the snowpack throughout the winter for each of the IMIS snow stations.
The following variables are measured or simulated in the standard programme of IMIS snow stations and are available in this dataset:

- Snow depth
- 24-hour new snow (SNOWPACK simulation)
- Air and surface temperature
- Wind speed and direction
- Relative humidity
- Reflected shortwave radiation
- Ground temperature
- Snow temperature 25 cm, 50 cm and 100 cm above the ground

 IMIS wind stations

Wind stations are generally situated at higher altitudes on exposed summits or ridges.
The following variables are measured in the standard programme of IMIS wind stations and are available in this dataset:

- Wind speed and direction
- Air temperature
- Relative humidity

When using the data, please consider and adhere to the associated [Terms of Use](https://www.slf.ch/en/services-and-products/data-and-monitoring/slf-data-service.html).

To download live data use our [API](https://measurement-api.slf.ch).

To download data older than 7 days use our [File Download](https://measurement-data.slf.ch).

automatic-weather-station

display_name: automatic-weather-station

imis

display_name: imis

measurement

display_name: measurement

new-snow

display_name: new-snow

snow

display_name: snow

en: IMIS measuring network


en: spruce-bark-beetle maturation-feeding life-table fecundity larvae ips-typographus

en: Ips life tables

en: See ReadMe

en: Ips typographus was reared in climate chambers at constant temperatures of 12, 15, 20, 25, 30 and 33°C. Developmental times from egg to teneral beetle stages and daily oviposition of females from preoviposition phase to their death were recorded. From these data life tables were computed and the data were used for modelling.

fecundity

display_name: fecundity

ips-typographus

display_name: ips-typographus

larvae

display_name: larvae

life-table

display_name: life-table

maturation-feeding

display_name: maturation-feeding

spruce-bark-beetle

display_name: spruce-bark-beetle

en: Temperature-dependent development and oviposition of the spruce bark beetle Ips typographus


en: photogrammetry wingtra dsm drone-data uav

en: Data Access

en:
- DSM 10cm resolution
- Orthomosaic 3cm resolution
- Agisoft Metashape Processing Report
- original RGB images

All generated products are also available as a cloud optimized geotiff.

en: We conducted four drone flights in Davos Wolfgang Arelen, in 2020/21 and 2022 to obtain data for the generation of DSMs and orthomosaics at a high resolution. The data was processed with the Agisoft Metashape Professional Software.

drone-data

display_name: drone-data

dsm

display_name: dsm

photogrammetry

display_name: photogrammetry

uav

display_name: uav

wingtra

display_name: wingtra

educ

en: Education, culture and sport

envidat

en: EnviDat: the Environmental Data Portal

en: Photogrammetric Drone Data Wolfgang Arelen


en: efa biogas mfa sfa circular-economy

en: Agricultural biogas plants in the circular economy - supplementary material

en:
This excel file contains:
-The summary of all values used for the inputs biomass characterisitcs based on literature.
-All input data for the flow analysis preformed with the programme STAN.
-Results tables

format: XLS

en:
Supplementary material for the publication " Agricultural biogas plants as a hub to foster circular economy and bioenergy: An assessment using material substance and energy flow analysis" Burg, V., b, Rolli, C., Schnorf, V., Scharfy, D., Anspach, V., Bowman, G.

Today's agro-food system is typically based on linear fluxes (e.g. mineral fertilizers importation), when a circular approach should be privileged. The production of biogas as a renewable energy source and digestate, used as an organic fertilizer, is essential for the circular economy in the agricultural sector. This study investigates the current utilization of wet biomass in agricultural anaerobic digestion plants in Switzerland in terms of mass, nutrients, and energy flows, to see how biomass use contributes to circular economy and climate change mitigation through the substitution effect of mineral fertilizers and fossil fuels. We quantify the system and its benefits in details and examine future developments of agricultural biogas plants using different scenarios. Our results demonstrate that agricultural anaerobic digestion could be largely increased, as it could provide ten times more biogas by 2050, while saving significant amounts of mineral fertilizer and GHG emissions.

biogas

display_name: biogas

circular-economy

display_name: circular-economy

efa

display_name: efa

mfa

display_name: mfa

sfa

display_name: sfa

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: Agricultural biogas plants as a hub to foster circular economy and bioenergy: An assessment using substance and energy flow analysis


en: strategic-plan governance landscape-principles plan-evaluation green-infrastructure

en: o	Detailed description of all the protocol items used to conduct the analysis and the way each question was coded

en: Coding results

en: o	Results of the coding procedure. Data were used to create Figures 2, 3, 4, 5, 6 and to qualitatively present the results in the research paper.

en:
The present dataset is part of the published scientific paper Hersperger, A.M., Bürgi, M., Wende, W., Bacău, S. and Grădinaru, S.R., 2020. Does landscape play a role in strategic spatial planning of European urban regions?. Landscape and Urban Planning, 194, p.103702.

The goal of this research was to assess the role of landscape in contemporary strategic spatial planning. In order to assess the role of “landscape” in the strategic spatial plans, we focused on how plans took advantage of landscape’s integrative power, how plans are based on knowledge on functioning of landscape systems, and how plans show the contribution of landscapes to human well-being. For each aspect, a number of items (detailed in Table 1 of the paper) were selected to assist the assessment.
This study is based on content analysis of the strategic spatial plans of 18 European urban regions. The strategic spatial plans were retrieved from the planning authorities’ websites. The cases study regions as well as the analyzed strategic spatial plans are presented in Table 2 of the paper.
The authors developed a protocol containing 28 items, out of which 16 were directly derived from information presented in Table 1. As a result, we provide the following outputs:
•	Protocol_items.docx – freely available - Detailed description of all the protocol items used to conduct the analysis.
•	Coding results.xlsx – available on request - Results of the coding procedure. Data were used to create Figures 2, 3, 4, 5, 6 and to qualitatively present the results in the research paper.

governance

display_name: governance

green-infrastructure

display_name: green-infrastructure

landscape-principles

display_name: landscape-principles

plan-evaluation

display_name: plan-evaluation

strategic-plan

display_name: strategic-plan

en: Landscape in contemporary strategic spatial plans of European Urban regions


en: landslide-early-warning soil-temperature soil-water-matrix-potential soil-moisture soil-water-content

en: In-situ soil moisture measurements, Trub, 2021-2022

en:
Volumetric soil water content (m3 m-3), soil water potential (mbar) and soil temperatures (oC) measured in two profiles and four depths each, as well as air temperature (oC) and precipitation (mm). Time intervall: 1 hour. Measurement period: April 2021-Dec 2022.
Location: slope, meadow
For a detailed description of site, soil and vegetation: see attached document.

en: In-situ soil moisture measurements, Ranflüh, 2021-2022

en:
Volumetric soil water content (m3 m-3), soil water potential (mbar) and soil temperatures (oC) measured in two profiles and four depths each, as well as air temperature (oC) and precipitation (mm). Time intervall: 1 hour. Measurement period: April 2021-Dec 2022.
Location: hillslope, meadow
For a detailed description of site, soil and vegetation: see attached document.

en: In-situ soil moisture measurements, Langnau i E, 2021-2022

en:
Volumetric soil water content (m3 m-3), soil water potential (mbar) and soil temperatures (oC) measured in two profiles and four depths each. Meteorological variables, such as air temperature or precipitation can be received from MeteoSwiss.
Time intervall: 1 hour. Measurement period: June 2021-Dec 2022.
Location: flat terrain, meadow (measurement site of MeteoSwiss)
For a detailed description of site, soil and vegetation: see attached document.

en: Detailed description of soil moisture measurment sites, soil properties and sensor installations (in German)

en: In-situ soil moisture measurements, Wasen i.E., flat location, 2019-2022

en:
Volumetric soil water content (m3 m-3), soil water potential (mbar) and soil temperatures (oC) measured in two profiles and four depths each, and two additional soil temperature measurements (oC), air temperature (oC) and precipitation (mm). Time intervall: 1 hour. Measurement period: April 2019-Dec 2022.
Location: flat terrain, meadow
For a detailed description of site, soil and vegetation: see attached document.

en: In-situ soil moisture measurements, Napf, 2021-2022

en:
Volumetric soil water content (m3 m-3), soil water potential (mbar) and soil temperatures (oC) measured in two profiles and four depths each. Meteorological variables such as air temperature or precipitation can be received from MeteoSwiss.
Time intervall: 1 hour.
Measurement period: June 2021-Dec 2022.
Location: flat terrain, meadow (official MeteoSwiss station)
For a detailed description of site, soil and vegetation: see attached document.

en: In-situ soil moisture measurements, Wasen i.E., steep slope, 2019-2022

en:
Volumetric soil water content (m3 m-3), soil water potential (mbar) and soil temperatures (oC) measured in two profiles and four depths each, and two additional soil temperature measurements (oC), air temperature (oC) and precipitation (mm). Time intervall: 1 hour. Measurement period: April 2019-Dec 2022.
Location: steep hillslope, meadow
For a detailed description of site, soil and vegetation: see attached document.

en: In the context of landslide early warning research, soil moisture (e.g. volumetric soil water content and soil water potential) has been measured at six locations in the Napf-region (Emmental, central Switzerland) since April 2019. Here, we provide the hourly mean values of all sensors from all 6 locations after a comprehensive data control, filtering and aggregation (from 10-min to 1-hour values). A sub-set of these data (for the locations Wasen i.E.) has previously been published in envidat.ch at https://www.doi.org/10.16904/envidat.369 applying the same data post-processing method. The dataset is complemented with meteorological data (locally measured air temperature and precipitation) as well as soil temperature. A detailed description of the sites and measurement installations can be found in a separate report (attached with the data).

landslide-early-warning

display_name: landslide-early-warning

soil-moisture

display_name: soil-moisture

soil-temperature

display_name: soil-temperature

soil-water-content

display_name: soil-water-content

soil-water-matrix-potential

display_name: soil-water-matrix-potential

en: In-situ soil moisture measurements Napf-region 2019-2022


en: soil-moisture soil-water-content icp-forests long-term-forest-ecosystem-research swiss-forest-lab

en: Data Request

en:
Continuous measurement of soil water content at 15, 50 and 70 cm depth in Visp (3 replications) with TDR soil moisture probes (Tektronix 1502 B) from 2001 until 25.04.2013

 Purpose:

Improve the available data for the calibration or validation of the water balance models, i.e. the determination of the water flux needed for calculating the leaching fluxes.

icp-forests

display_name: icp-forests

long-term-forest-ecosystem-research

display_name: long-term-forest-ecosystem-research

swiss-forest-lab

display_name: swiss-forest-lab

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: TDR soil water content measurements LWF Visp


maintainer: Christian G. Sommer

en: wind-packing kinect wind-crust snow wind-tunnel

en: Kinect data

en: Links to the dataset

en: Processing scripts

en: Contains the Matlab- and R-scripts used to process the Kinect data

en: README

media_type: text/plain

en: Describes the dataset in detail

format: TXT

mimetype: text/plain

en:
This data sets contains the Microsoft Kinect data from 15 wind tunnel experiments on wind-packing / wind crust formation. These experiments were performed in the winter 2016/17. The Kinect measures distributed snow depth.

The Kinect data is organized per experiment. Each experiment subfolder contains the processed Kinect depth images and some additional files.

Please refer to the README for more details on the data. The processing scripts are available for download as well. The scripts are mainly provided as documentation and would need to be adjusted to be used.

This dataset is the basis of the following publication:

Sommer C.G., Lehning M. & Fierz C. (2018). Wind Tunnel Experiments: Influence of Erosion and Deposition on Wind-Packing of New Snow. Front. Earth Sci. 6:4. doi: 10.3389/feart.2018.00004

kinect

display_name: kinect

snow

display_name: snow

wind-crust

display_name: wind-crust

wind-packing

display_name: wind-packing

wind-tunnel

display_name: wind-tunnel

en: Wind crust formation: Microsoft Kinect data


en: analytical-hierarchy-process strategic-planning planning-efficacy land-use-planning governance

en: The present content is part of the published paper Palka, G., Oliveira, E., Pagliarin, S., & Hersperger, A. M. (2021). Strategic spatial planning and efficacy: an analytic hierarchy process (AHP) approach in Lyon and Copenhagen. European planning studies, 29(6), 1174-1192. It contains the interviews, the survey, the report explaining survey and a xlxs table to save results.

analytical-hierarchy-process

display_name: analytical-hierarchy-process

governance

display_name: governance

land-use-planning

display_name: land-use-planning

planning-efficacy

display_name: planning-efficacy

strategic-planning

display_name: strategic-planning

en: Planning efficacy - questionnaire and interviews


en: Additional publications

media_type: text/html

format: HTML

en: Request Data

en: This dataset is hosted by IAP and therefore, access to the dataset must be requested to the original data provider.

en:
The IAP has been monitoring forest health since 1984 on behalf of cantonal forest and environmental offices and in collaboration with the Federal Office for the Environment. In the Intercantonal Forest Observation Program (WDB) project, the health, growth and nutrient supply of beech, spruce and oak in managed forest ecosystems are studied on about 190 forest plots. The plots cover the most important gradients of Swiss forests, such as different climatic conditions in precipitation, temperature, as well as differences in soil and in the input of air pollutants such as nitrogen and ozone. Currently (date 2020) 94 plots with 6268 beech trees, 75 plots with 4547 spruce trees, and 50 plots with 1858 oak trees are surveyed in the Intercantonal WDB. Annual investigations include crown condition and tree loss by mortality, uprooting and stem breakage. Every 4 year stem increment is measured on all 12’673 trees and 8 branches are harvested by helicopter very 4 years and subsequently examined for the following parameters:

- Nutrient analysis in foliage (N, P, K, Ca, Mg, Mn)
- Leaf area and weight
- Shoot growth (retrospective for Norway spruce, beech and oak)
- Discoloration and parasite infestation
- Fructification of beech (retrospectively)

In addition, soil samples for analysing the chemistry of the solid phase are taken every 12 years. Also changes in the ground vegetation is assessed every 12 years. On a subset of the plots soil solution is sampled monthly *[(Soil solution monitoring of the Intercantonal Forest Observation Program)](https://www.envidat.ch/dataset/soil-solution-monitoring-of-the-intercantonal-forest-observation-program)*. In addition, soil water potential and soil moisture are measured in a subset of sites of the Intercantonal Forest Observation Program *[(Soil moisture and soil water potential measurements of the Intercantonal Forest Observation Program)](https://www.envidat.ch/dataset/soil-water-measurements-wdb)*.

These data allow to gain a unique understanding of the main factors influencing the forest and the most important changes, which are very valuable especially in the context of climate change. The insights are of great importance for cantonal and regional forest planning as well as for national and international determinations of critical loads and limits (e.g. CLempN, UNECE CLRTAP).

iap

display_name: iap

long-term-data-sets

display_name: long-term-data-sets

long-term-monitoring

display_name: long-term-monitoring

wdb

display_name: wdb

en: Intercantonal Forest Observation Program – Interkantonale Walddauerbeobachtung (WDB)


en: green-economy bioeconomy circular-economy forest-clearances atree sustainable-economy

en:
The data consistes of three colums as described below and the rows contain all the forest clearance requests and decisions between 2001 and 2017:

First column

The ID of the forest clearance request, which is also contained in the related dataset available from FOEN

Second column

The sustainable economy content class of a forest clearance request: G = green economy, C = circular economy, GB = green and bioeconomy, GC = green and circular economy, GCB = green and circular bioeconomy. If a cell is empty, the content was not codable as "sustainable economy" related.

Third column

The type of infrastructure project: if based on the description of the forest clearnce request it was necessary to change the field "type of infrastructure", so the clearance could be attributed to the correct class, this is indicated in this third column.

en: The Federal Office for the Environment (FOEN) is responsible for granting exemptions for forest clearances that in principle are prohibited in Switzerland. Initiators of infrastructure projects have to submit an examption approval request to the cantonal forest administration which has to inform the FOEN. The FOEN thus administers a dataset of forest clearance requests and approval decisions that can be requested there. This dataset contains information on a coding of the content of all the forest clearance requests between 2001 and 2017, that elicits whether the reason for the clearance can be attributed to "sustainable economy" objectives such as "green economy", "bioeconomy" and "circular economy".

atree

display_name: atree

bioeconomy

display_name: bioeconomy

circular-economy

display_name: circular-economy

forest-clearances

display_name: forest-clearances

green-economy

display_name: green-economy

sustainable-economy

display_name: sustainable-economy

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: Content coding of exemption approval decisions for forest clearances


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

en: Data Access via S3

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

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

format: GeoTIFF

en: Technical documentation

en: Technical documentation containing file metadata and variable descriptions.

air-temperature

display_name: air-temperature

glaciers

display_name: glaciers

last-glacial-maximum

display_name: last-glacial-maximum

orography

display_name: orography

paleo-climate

display_name: paleo-climate

precipitation

display_name: precipitation

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


maintainer: Frank Techel

en: snow observations alps shapefile avalanches

en: Selected wet snow avalanche activity data Davos, Switzerland (2011-2014)

en: Zip archive with shapefiles for the selected wet snow avalanche polygons, including metadata.

en:
Polygons of wet snow avalanches in the Davos area, as documented by the Swiss avalanche warning service. The georeferenced outlines of the avalanches contain both the release as well as the deposit area, but without separating between both.

The dataset is a subset of the total record of 1615 avalanches classified as wet snow avalanches from October 2011 - September 2014, containing those 255 avalanches exceeding 0.0125 km^2. Every polygon comes with meta data, including the date of occurrence.

This dataset is the underlying dataset to:
Wever, N., Vera Valero, C. and Techel, F. (2018) _Coupled snow cover and avalanche dynamics simulations to evaluate wet snow avalanche activity_. Submitted to J. Geophys. Res., in review.

alps

display_name: alps

avalanches

display_name: avalanches

observations

display_name: observations

shapefile

display_name: shapefile

snow

display_name: snow