maintainer: Anita Risch

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

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


maintainer: EnviDat Support

en: spatially-distributed-sampling stream-water geochemical-solutes stable-water-isotopes precipitation

state: active

type: dataset

format: XLS

en: The dataset contains daily measurements of volumes, isotopes and solutes of stream water as well as precipitation measured several locations; meteorological variables are added. Date: 18.07.2019

en:
This dataset contain measurements of solute and stable water isotopes in stream water and precipitation in the Alp catchment and two of its tributaries (between 2015 -2018) . The river Alp is a snow-dominated catchment situated in Central Switzerland characterized by an elevation range from 840 to 1898 m a.s.l. The dataset provides solutes (major anions and cations, trace metals) and stable water isotopes and water fluxes (precipitation rates, discharge) at daily intervals from several sampling locations.
An updated version of the isotope dataset is available here: https://www.doi.org/10.16904/envidat.242

geochemical-solutes

display_name: geochemical-solutes

precipitation

display_name: precipitation

spatially-distributed-sampling

display_name: spatially-distributed-sampling

stable-water-isotopes

display_name: stable-water-isotopes

stream-water

display_name: stream-water

education

fr: Education, science

de: Bildung, Wissenschaft

en: Education and science

it: Formazione e scienza

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: Daily data of solute and stable water isotopes in stream water and precipitation in the Alp catchment, Central Switzerland


maintainer: Felix Neff

en: restoration insects topsoil-removal functional-traits diversity grassland long-term-experiment functional-diversity

en: Insect abundance

media_type: text/csv

en:
Abundance of adult insects recorded in the samplings on all experimental sites

- **Plot**: ID of Plot
- **Treatment**: Experimental treatment
- **Species**: Insect species name (following [Fauna Europaea](https://fauna-eu.org))
- **Author**: Author and year of species' description (following [Fauna Europaea](https://fauna-eu.org))
- **Group**: Insect group as used in the analyses
- **Number_Adults**: Number of adult individuals recorded
- **Herbivore**: Logical indicating whether the species is feeding as a herbivore (*TRUE*) or not (*FALSE*)

format: CSV

mimetype: text/csv

en: Insect traits

en:
Functional traits of all herbivorous insect species sampled in the study.

- **Species**: Insect species name (following [Fauna Europaea](https://fauna-eu.org))
- **Author**: Author and year of species' description (following [Fauna Europaea](https://fauna-eu.org))
- **Group**: Insect group as used in the analyses
- **Body volume**: Body volume determined by body length, body width and body height (in mm$^3$)
- **Body_shape**: Ratio of body length to body width
- **Hind_femur_shape**: Ratio of hind-femur length to hind-femur width
- **Hind_front_leg_ratio**: Ratio of front-leg length to hind-leg length (leg length = femur length + tibia length)
- **Wing_length_rel**: Ratio of wing length to body length
- **Leg_length_rel**: Ratio of front-leg length to body length (leg length = femur length + tibia length)
- **Antenna_length_rel**: Ratio antenna length to body length
- **Eye_width_rel**: Ratio of eye width to head width (Auchenorrhyncha, Heteroptera) / to head height (Orthoptera)
- **Feeding_specialization**: Insect specialization on food source (*m*: monophagous, *o*: oligophagous, *p*: polyphagous)
- **Feeding_tissue**: Feeding tissue used for feeding (*c*: chewers, *x*: xylem, *p*: phloem, *m*: mesophyll, *m-p/r*: mesophyll as well as phloem and/or reproductive organs, *r*: reproductive organs, *se*: ripe seeds)
- **Hibernation**: Hibernation stage (*e*: egg, *e/n*: egg and nymph, *n*: nymph, *a*: adult)
- **Generations**: Number of generations per year (*1.5* stands for *1-2* generations per year)
- **Moisture_pref_mean**: mean of preferred habitat moistures (*1*: xerophilous, *2*: moderately xerophilous, *3*: moderately mesohygrophilous, *4*: mesohygrophilous, *5*: moderately hygrophilous, *6*: hygrophilous, *7*: moderately hydrophilous, *8*: hydrophilous)
- **Moisture_pref_range**: range of preferred habitat moistures (indicating degree of specialization)

en: Plot information

en:
Information on the experimental plots.

- **Plot**: ID of Plot
- **Treatment**: Experimental treatment
- **Landuse_history**: recent agricultural use for Initial; agricultural use before restoration for all restored sites
- **Last_tilled**: Last time the site was tilled
- **Intensity**: Frequency and intensity of mowing and manuring (*intensity1*: mowing once and no manure, i*ntensity2*: 2-3 times mowing and no manure, *intensity3*: 2-3 times mowing and manuring, *intensity4*: 4-5 times mowing and manuring)
- **Slope**: slope gradient according to classes defined by FAO (1990)
- **X**: X coordinate of the plot (CH1903)
- **Y**: Y coordinate of the plot (CH1903)
- **Cluster**: Spatial cluster of the plot

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

**Paper Citation**:

Neff, F., Resch, M. C., Marty, A., Rolley, J. D., Schütz, M., Risch, A. C, Gossner, M. M. Accepted. Long-term restoration success of insect herbivore communities in semi-natural grasslands: a functional approach. Ecological Applications.

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

 Methods

 Study site
The study area is situated within and nearby to Eigental nature reserve (47°27’36” to 47°29’06” N, 8°37’12” to 8°37’44” E, 461 to 507 m a.s.l.) in the vicinity of Zurich airport (Canton Zurich, Switzerland). Mean annual precipitation and temperature is 903 ± 136 mm and 9.14°C ± 0.50°C (mean ± SD for 2007-2017 (*MeteoSchweiz 2018*)). In 1967, the Eigental nature reserve was established to protect small and isolated remnants of species-rich, semi-natural grasslands (roughly 12 ha), which were embedded in an otherwise intensively managed landscape. It is characterized by oligo- to mesotrophic Molinion (semi-wet, matrix species *Molinia caerulea*) and Mesobromion (semi-dry, matrix species *Bromus erectus*) meadows (*Delarze et al. 2015*), reflecting small-scale habitat heterogeneity, mainly due to site-specific groundwater levels and slope inclination. As in most Central European grasslands, management is necessary to prevent shrub and tree invasions as well as to secure low levels of available soil nutrients and thus to maintain these species-rich habitats ([*Poschlod and WallisDeVries 2002*](https://doi.org/10.1016/S0006-3207(01)00201-4)).
In 1990, the government of the Canton Zurich decided to enlarge the Eigental nature reserve as a counter measure against degradation and biodiversity loss in semi-natural grasslands due to overutilization and the excessive input of nutrients (mostly nitrogen). Eleven patches of adjacent intensively managed grassland (in total roughly 20 ha) were targeted to be transformed into semi-natural grasslands. As a first restoration measure, fertilization was ceased, and biomass harvested three times to remove excessive soil nutrients from the original system and thus benefit plant species with low competitive ability on the long run. In 1995, the restoration efforts were increased and a large-scale experiment comprising three restoration measures with increasing intervention intensities was implemented:

- **Harvest only**: Initial restoration measures were continued with mowing and removing of the aboveground biomass two times a year (early summer and autumn).
- **Topsoil**: Removal of topsoil, depending on the thickness of the A horizon the upper 10 to 20 cm, in four randomly selected areas within the eleven patches in late autumn 1995. The size of the restoration area depended on individual patch size (2700 to 7000 m2).
- **Topsoil + Propagules**: Plant propagules were added on half of the area where topsoil was removed via application of fresh, seed-containing hay and hand-collected propagules of target species originating from semi-dry and semi-wet species-rich grasslands with local and regional provenance (within radius of 7 to 30 km) (1995, 1996, 1997).

Management of *Topsoil* and *Topsoil + Propagules* started five years after treatment implementation and included yearly mowing and removing of aboveground biomass (late summer or early autumn). The experiment was complemented with intensively managed grassland sites that share the same agricultural history as the restored sites (**Initial**; swards dominated by *Lolium perenne*, *L. multiflorum* and *Trifolium repens*): mowing and subsequent fertilizing (manure) up to five times a year, as well as different tillage regimes. Finally, sites were selected in target semi-dry and semi-wet grasslands (**Target**) located within the Eigental nature reserve and another nature reserve nearby (Altläufe der Glatt; 47°28’29” to 47°27’41” N, 8°31’56” to 8°32’26” E, 418 to 420 m a.s.l.). The selected target sites are mown and aboveground biomass removed once a year in late summer or early autumn. For each of the five treatments, we selected eleven plots (5 m × 5 m) spread across the sites. Altogether, the experiment included 55 plots.

 Arthropod sampling
Aboveground arthropods were sampled using suction sampling on four consecutive days in early July 2017 before the grasslands were mown. Arthropods were sampled in two locations on each 5 m × 5 m plot, once in the south-western and once in the north-eastern corner to account for possible spatial heterogeneity within the plots. Arthropods were sorted to order or lower taxonomic levels and individuals were identified to species level. We focused on three groups (Hemiptera: Auchenorrhyncha, Hemiptera: Heteroptera, Orthoptera),

 Functional traits
We used two sets of functional traits in this study.

**Morphometric traits**:
Body volume, body shape, hind femur shape, hind/front leg ratio, wing length, leg length, antenna length and eye width. We used trait measurements from [*Simons et al. (2016)*](http://dx.doi.org/10.1890/15-0616.1) and [*Neff et al. (2019)*](https://doi.org/10.1007/s10980-019-00872-1) and complemented them with measurements on study specimens. These measurements were conducted using a high-resolution measuring stereo microscope (Leica DVM6, Leica Microsystems) including automated high-resolution photo stacking with the software Leica Application Suite X (LAS X, © 2018 Leica Microsystems CMS GmbH) and Leica Map Premium (Leica Microsystems, © 1996-2017 Digital Surf) at WSL Birmensdorf. The eight morphometric traits were calculated from direct measurements of body parts on specimens of all sampled species. From each species, we measured at least one female and one male specimen. Additionally, for species that show wing dimorphism, we included the different wing morphs and weighted them by their prevalence reported in literature. For few species, of which not all wing morphs were available for measurements (10 cases), we estimated relative wing length from congeneric species or from the literature.

**Life-history traits**
Based on an existing data set collected by [*Gossner et al. (2015)*](http://dx.doi.org/10.1890/14-2159.1). We included traits describing different life-history characteristics of herbivore insect species, namely: feeding specialization, feeding tissue, hibernation stage and number of generations per year, which are related to insect species’ vulnerability to changes in plant community composition, microhabitat use and disturbance tolerance. To represent potential changes in habitat moisture with abandonment of intensive land use (e.g., change in ground-water level), we also included two traits related to preferred habitat moisture of the study species: moisture preference, describing species’ optimum habitat moisture, and moisture range, which describes the species’ range of preferable moisture conditions.

 References

Delarze, R., Y. Gonseth, S. Eggenberg, and M. Vust. 2015. Lebensräume der Schweiz: Ökologie - Gefährdung - Kennarten. 3rd ed. Ott, Bern.

Gossner, M. M., N. K. Simons, R. Achtziger, T. Blick, W. H. O. Dorow, F. Dziock, F. Köhler, W. Rabitsch, and W. W. Weisser. 2015. A summary of eight traits of Coleoptera, Hemiptera, Orthoptera and Araneae, occurring in grasslands in Germany. Scientific Data 2:150013.

MeteoSchweiz. 2018. Klimabulletin Jahr 2017. MeteoSchweiz, Zürich.

Neff, F., N. Blüthgen, M. N. Chisté, N. K. Simons, J. Steckel, W. W. Weisser, C. Westphal, L. Pellissier, and M. M. Gossner. 2019. Cross-scale effects of land use on the functional composition of herbivorous insect communities. Landscape Ecology 34:2001–2015.

Poschlod, P., and M. F. WallisDeVries. 2002. The historical and socioeconomic perspective of calcareous grasslands—lessons from the distant and recent past. Biological Conservation 104:361–376.

Simons, N. K., W. W. Weisser, and M. M. Gossner. 2016. Multi-taxa approach shows consistent shifts in arthropod functional traits along grassland land-use intensity gradient. Ecology 97:754–764.

diversity

display_name: diversity

functional-diversity

display_name: functional-diversity

functional-traits

display_name: functional-traits

insects

display_name: insects

long-term-experiment

display_name: long-term-experiment

restoration

display_name: restoration

topsoil-removal

display_name: topsoil-removal

en: Grassland restoration: insects and insect traits


maintainer: Matthias Haeni

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

en: Data plot of the forest station (ALB)

media_type: application/pdf

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

format: PDF

mimetype: application/pdf

en: Forest station data (ALB)

en: Site aerial photo (Alpthal)

media_type: image/jpeg

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

format: SERVICE

mimetype: image/jpeg

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

climate-change

display_name: climate-change

long-term

display_name: long-term

meteo

display_name: meteo

meteorology

display_name: meteorology

par

display_name: par

relative-humidity

display_name: relative-humidity

swiss-forest-lab

display_name: swiss-forest-lab

temperature

display_name: temperature

wind-speed

display_name: wind-speed

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


maintainer: Fachstelle Open Government Data des Kantons Zürich

de: ZH Datasets Visits - 2020 Januar

de: ZH Datasets Visits - 2020 März

de: ZH Datasets Visits - 2019 Juni

de: ZH Datasets Visits - 2018 April

de: ZH Datasets Visits - 2020 April

de: Ausgenommen sind die Datensätze, die von der Geoinformation des Kantons Zürich auf opendata.swiss verwaltet werden.

de: ZH Datasets Visits - 2018 März

de: ZH Datasets Visits - 2018 Mai

de: ZH Datasets Visits - 2019 Juli

de: ZH Datasets Visits - 2019 Oktober

de: ZH Datasets Visits - 2018 Februar

de: ZH Datasets Visits - 2019 April

de: ZH Datasets Visits - 2020 November

de: ZH Datasets Visits - 2019 Mai

de: ZH Datasets Visits - 2018 November

de: Ausgenommen sind die Datensätze, die von der Geoinformation des Kanton Zürich auf opendata.swiss verwaltet werden.

de: Monatliche Nutzungsstatistiken (Anzahl Besuche) der Open Government Data (OGD) Metadatensätze von Verwaltungseinheiten und Organen des Kantons Zürich, die auf dem zentralen Katalog für offene Behördendaten opendata.swiss findbar sind. Hinweise: Ab Januar 2019 sind die Web Analytics um weitere Metadateninformationen erweitert bzw. wurden Metadatenanpassungen vorgenommen. Ab März 2021 sind die monatlichen Aktualisierungen aufgrund technischer Herausforderungen pausiert. Variabelndefinitionen: Column 'name' = dataset slug; 'issued' = first publication of dataset; 'organization_name' = publisher slug; 'organization_url' = publisher URL; 'E' up to 'AB' = thematic categories according to DCAT AP Switzerland.

fachstelle-ogd-kanton-zuerich

de: Fach- und Koordinationsstelle Open Government Data Kanton Zürich

de: Die Fach- und Koordinationsstelle Open Government Data (OGD) ist das kantonale Kompetenzzentrum für offene Behördendaten im Statistischen Amt. Wir unterstützen die Organisationseinheiten und Organe des Kantons bei der Bereitstellung ihrer nicht schützenswerten Daten als Open Data.

de: Web Analytics der Open Government Data des Kantons Zürich auf opendata.swiss von Februar 2018 bis Februar 2021


lidar-davos-wolfgang

maintainer: Patric Seifert

title_for_slug: lidar-davos-wolfgang

en: polly raclets clouds tropos lidar

en: Raman Lidar Davos

en: A portable Raman lidar system (Polly) from Leibnitz Institute for Tropospheric Research (Tropos) was deployed at Davos Wolfgang (LON: 9.853594, LAT: 46.835577). Please use this [link](http://polly.tropos.de/?p=lidarzeit&Ort=39), to be directly forwarded to the Davos location and select the date of interest from the calendar (bold numbers). The data can be requested directly at the Polly team.

clouds

display_name: clouds

lidar

display_name: lidar

polly

display_name: polly

raclets

display_name: raclets

tropos

display_name: tropos

education

de: Bildung, Wissenschaft

en: Education and science

envidat

de: EnviDat: das Umwelt-Datenportal

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.

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.

en: LIDAR Davos Wolfgang


en: drifting-snow mass-flux terrestrial-laser-scanning snowmicropen meteorological-data antarctica

en: README

media_type: text/plain

en: Describes the dataset in detail

format: TXT

mimetype: text/plain

en: Dataset

media_type: Link

en: Links to the dataset

en:
This dataset contains the data acquired during the expedition to Princess Elisabeth Antarctica Station in December 2016 and January 2017. The dataset consits of meterorological data, drifting snow mass flux data, SnowMicroPen data and Terrestrial Laser Scanning data.

Please refer to the README for more information about the data.

This dataset is the basis of the following publication:

Sommer, C. G., Wever, N., Fierz, C., and Lehning, M.: Wind-packing of snow in Antarctica, The Cryosphere Discuss., https://doi.org/10.5194/tc-2018-36, in review, 2018.

antarctica

display_name: antarctica

drifting-snow

display_name: drifting-snow

mass-flux

display_name: mass-flux

meteorological-data

display_name: meteorological-data

snowmicropen

display_name: snowmicropen

terrestrial-laser-scanning

display_name: terrestrial-laser-scanning

en: Expedition to Princess Elisabeth Antarctica Station, 2016/2017


maintainer: Giulia Mazzotti

en: snow-distribution forest-structure forest-snow snow-energy-balance snow-modelling

en: Canopy data

en: Includes all canopy structure metrics computed at all surveyed locations

en: Coordinates data

en: Includes coordinate information of each surveyed point (7 x 276 = 1932 forest points, 2 open areas)

en: Snow depth data open sites

en: Contains all snow detph data accquired at open sites nearby the forest stands during the same period.

en: Snow depth data forest sites

en: Contains all snow depth data acquired at all forest sites during winters 2012/13, 2013714 and 2014/15.

en: Meteo data to drive FSM2 model

media_type: application/zip

en: Includes meteorological driving data used to run the forest snow model FSM2, processed and parsed in text files that match the format required by FSM2. Separate files are available for each field area (Laret, Drusatscha and Ischlag) and season (2012/13, 2013/14, 2014/15). Each file includes data for the period from October 1st to May 31st at hourly resolution.

format: ZIP

mimetype: application/zip

en: Grid point nomenclature

en: The grid structure of each forest site and the respective nomenclature applied to label individual points within each grid are outlined here.  Each point marks the location of snow depth measurements and co-located canopy structure parameters.

en:
This dataset contains all snow, canopy and meteorological data presented and used in the publication: Mazzotti, G., Essery, R., Moeser, D. & Jonas T. (2020) 'Resolving spatial variability of forest snow using an energy-balance model with a 1-layer canopy'. Water Resources Research, https://doi.org/10.1029/2019WR026129.
This publication must be cited when using this dataset.

forest-snow

display_name: forest-snow

forest-structure

display_name: forest-structure

snow-distribution

display_name: snow-distribution

snow-energy-balance

display_name: snow-energy-balance

snow-modelling

display_name: snow-modelling

en: Snow depth, canopy structure and meterorological datasets from the Davos area, Switzerland, Winters 2012/13-2014/15, used for high-resolution forest snow modelling


maintainer: Elisabeth Hafner

en: snow satellite avalanche avalanche-hazard-mapping validation

en: Satellite Avalanche Mapping Validation data and data description

media_type: ZIP

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

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

Coordinate system: CH1903+_LV95

The generation of this dataset is described in detail in:

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

avalanche

display_name: avalanche

avalanche-hazard-mapping

display_name: avalanche-hazard-mapping

satellite

display_name: satellite

snow

display_name: snow

validation

display_name: validation

education

en: Education and science

envidat

en: EnviDat: the Environmental Data Portal

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

en: Satellite avalanche mapping validation data


en: studibach switzerland alptal groundwater time-series

en:
Groundwater time series of the monitoring network in the Studibach (C7) catchment, Alptal, Switzerland published in
Rinderer M., van Meerveld I, McGlynn B. (2019): From points to patterns – Assessing runoff source area dynamics and hydrological connectivity using time series clustering. Water Resources Research, doi: 2018WR023886R

en: Groundwater time series between 2010 and 2014 of the distributed monitoring system in the Studibach (C7), Alptal, Switzerland. Data published in Rinderer M., van Meerveld I, McGlynn B. (2019): From points to patterns – Assessing runoff source area dynamics and hydrological connectivity using time series clustering. Water Resources Research, doi: 2018WR023886R

alptal

display_name: alptal

groundwater

display_name: groundwater

studibach

display_name: studibach

switzerland

display_name: switzerland

time-series

display_name: time-series

en: Groundwater time series Studibach (Rinderer et al., 2019, WRR)


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

en: Site photo of the field station (ISF)

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

en: Site photo of the forest station (ISB)

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

en: Field station data (ISF)

en: Data file.

en: Forest station data (ISB)

en: Data plot of the field station (ISF)

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

en: Site aerial photo (Isone)

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

en: Data plot of the forest station (ISB)

en: High quality meteorological data are needed for long-term forest ecosystem research, particularly in the light of global change. The long-term data series published here comprises almost 20 years of measurements for two meteorological stations in Isone in Switzerland where one station is located within a natural broad-leaved forest stand (ISB) with European beech (_Fagus sylvatica_; 70-100 yrs) as dominant tree species. A second station is situated in the very vicinity outside of the forest (field station, ISF). The meteorological time series are presented in hourly time resolution of air temperature, relative humidity, precipitation, photosynthetically active radiation (PAR) and wind speed. Isone is part of the Long-term Forest Ecosystem Research Programme (LWF) established and maintained by the Swiss Federal Research Institute WSL.

climate-change

display_name: climate-change

long-term

display_name: long-term

meteo

display_name: meteo

meteorology

display_name: meteorology

par

display_name: par

precipitation

display_name: precipitation

relative-humidity

display_name: relative-humidity

swiss-forest-lab

display_name: swiss-forest-lab

temperature

display_name: temperature

wind-speed

display_name: wind-speed

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


causal-effect-of-mfoz

title_for_slug: causal-effect-of-mfoz

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

en: Data and Stata code for repeating the results

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

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

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

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

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

built-up-land-change

display_name: built-up-land-change

causality

display_name: causality

fujian-province

display_name: fujian-province

propensity-score-matching

display_name: propensity-score-matching

selection-bias

display_name: selection-bias

the-major-function-oriented-zone

display_name: the-major-function-oriented-zone

education

en: Education and science

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: Causal effect of MFOZ


maintainer: Achille Capelli

en: snow-water-equivalent liquid-water-content gps gnss snow swe lwc

en: Daily data for the site Weissfluhjoch at 2540 m a.s.l (46°49’47’’ N, 9°48’34’’E) for the two winters 2018-2020. These data were processed to daily values from the other data files.

en: Profile data for Laret at 1510 m a.s.l. (46°50’2’’N, 9°52’17’’E) for the two winter 2018-2020.

en: Snow profiles data from Klosters (1210 m a.s.l. ,46°51’49’’N, 9°53’17’’E) for the two winters 2018-2020.

en: Daily data from Küblis at 820 m a.s.l. (46°54’48’’N, 9°46’54’’E) for the two winters 2018-2020. These data were processed to daily values from the other data files.

en: Snow and meteo data from automatic sensors from Klosters (1210 m a.s.l. ,46°51’49’’N, 9°53’17’’E) for the two winters 2018-2020.

en: Daily data from Klosters (1210 m a.s.l. ,46°51’49’’N, 9°53’17’’E) for the two winters 2018-2020. These data were processed to daily values from the other data files.

en: Manual profiles

media_type: .zip

en: Data of the traditional manual profiles for the locations Weissfluhjoch, Klosters and Küblis. For the location of Küblis there are no traditional manual profile data. We provided the data as both PDF and .CAAML format (See https://niviz.org/ or http://caaml.org/Schemas/V5.0/Profiles/SnowProfileIACS/CAAMLv5_SnowProfileIACS.pdf). Moreover, we added LWC and density profiles when available (all locations).

en: Webcam images

en: Webcam images showing some typical differences in the snow conditions at the four sites (Küblis, Klosters, Laret and Weissfluhjoch) for two time periods (14-18.3.2019 and 27.1-11.2.2020). Both time periods included a precipitation event with partial rain-on–snow occurring at the lower locations.

media_type: .csv

en: GNSS derived data for Laret at 1510 m a.s.l. (46°50’2’’N, 9°52’17’’E) for the two winter 2018-2020.

en: Snow and meteo data from automatic sensors for Laret at 1510 m a.s.l. (46°50’2’’N, 9°52’17’’E) for the two winter 2018-2020.

en: Daily observer data from Küblis at 820 m a.s.l. (46°54’48’’N, 9°46’54’’E) for the two winters 2018-2020.

en: Snow and meteo data from automatic sensors from Küblis at 820 m a.s.l. (46°54’48’’N, 9°46’54’’E) for the two winters 2018-2020.

en: Snow and meteo data from automatic sensors for the site Weissfluhjoch at 2540 m a.s.l (46°49’47’’ N, 9°48’34’’E) for the two winters 2018-2020.

en: Snow profiles data for the site Weissfluhjoch at 2540 m a.s.l (46°49’47’’ N, 9°48’34’’E) for the two winters 2018-2020.

en: Daily data for Laret at 1510 m a.s.l. (46°50’2’’N, 9°52’17’’E) for the two winters 2018-2020. These data were processed to daily values from the other data files.

en: GNSS derived SWE, HS, and LWC for the site Weissfluhjoch at 2540 m a.s.l (46°49’47’’ N, 9°48’34’’E) for the two winters 2018-2020.

en: GNSS derived SWE, LWC and HS from Küblis at 820 m a.s.l. (46°54’48’’N, 9°46’54’’E) for the two winters 2018-20

en: Daily observer data for the site Weissfluhjoch at 2540 m a.s.l (46°49’47’’ N, 9°48’34’’E) for the two winters 2018-2020.

en: Daily observer data from automatic sensors from Klosters (1210 m a.s.l. ,46°51’49’’N, 9°53’17’’E) for the two winters 2018-2020.

en: GNSS derived SWE, LWC and HS from Klosters (1210 m a.s.l. ,46°51’49’’N, 9°53’17’’E) for the two winters 2018-20

en: Snow profiles data from Küblis at 820 m a.s.l. (46°54’48’’N, 9°46’54’’E) for the two winters 2018-2020.

en: This database contains GNSS derived snow water equivalent (SWE), liquid water content (LWC), and snow height (HS) and reference data collected during the two winter 2018-2020 at 4 sites Weissfluhjoch (2540 m asl, 46°49’47’’ N, 9°48’34’’E), Laret (1515 m asl, . 46°50’2’’N, 9°52’17’’E), Klosters (1200 m asl, 46°51’49’’N, 9°53’17’’E), and Küblis (815 m asl, 46°54’48’’N, 9°46’54’’E).

gnss

display_name: gnss

gps

display_name: gps

liquid-water-content

display_name: liquid-water-content

lwc

display_name: lwc

snow

display_name: snow

en: Snow water equivalent measurements with low-cost GNSS receivers along a steep elevation gradient in the East-ern Swiss Alps


snow-drift-station-snow-and-air-data

maintainer: Benjamin Walter

title_for_slug: snow-drift-station-snow-and-air-data

en: snow-height temperature raclets snow snow-temperature snow-depth

en: Snow Surface Temperature

en: The snow surface temperature (°C) was measured with a Campbell SI-111 at 0.7 m above ground. The time is given in UTC+1.

en: Snow Depth

en: The snow depth (cm) was measured with a Lufft SHM-31 which was mounted at 1.7 m above ground. The time is given in UTC+1.

en: Air Temperature

en: The air temperature (°C) was measured with a Campbell CS-215 which was mounted at a height of 2.2 m above ground. The time is given in UTC+1.

en: Relative Humidity

en: The relative humidity (%) was measured with a Campbell CS-215 at a height of 2.2 m above ground. The time is given in UTC+1.

en: Snow and air data was monitored at Gotschnagrat (LON: 46.859 LAT: 9.849) by an infrarot radiometer (Campbell SI-111) for snow temperature (°C), a snow height sensor (Lufft SHM-31) for snow height change (cm) and a temperature and humidity sensor (Campbell CS-215) for air temperature (°C) and relative humidity (%). No filter was applied to the sensors and the smapling frequency was 1 Hz.

raclets

display_name: raclets

snow-depth

display_name: snow-depth

snow-height

display_name: snow-height

snow-temperature

display_name: snow-temperature

education

en: Education and science

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: Snow Drift Station - Snow and Air Data


maintainer: Ionuț Iosifescu Enescu

en: Bulk Data Access

en: Link to the S3 bucket where all the data resources can be downloaded in bulk

en: map 1GB

media_type: image/tiff

format: TIFF

mimetype: image/tiff

en: large map 10GB

en: huge map 100GB

en: map preview 0.5MB

en: map 0.5GB

en: map 0.2GB

en: map 2GB

en:
The attached data are some large GIS raster files (GeoTIFFs) made with Natural Earth data. Natural Earth is a free vector and raster map data @ naturalearthdata.com. The data used for creating these large files was the "Cross Blended Hypso with Shaded Relief and Water". Data was concatenated to achieve larger and larger files. Internal pyramids were created, in order that the files can be opened easily in a GIS software such as QGIS or by a (future) GIS data visualisation module integrated in EnviDat.

Made with Natural Earth. Free vector and raster map data @ naturalearthdata.com

gis

display_name: gis

large-files

display_name: large-files

natural-earth

display_name: natural-earth

qgis

display_name: qgis

en: Large GIS raster data derived from Natural Earth Data (Cross Blended Hypso with Shaded Relief and Water)


en: arctic ice sea-salt-aerosol antarctica snow

en: Fig 1F

en: Data to Figure 1F

en: Fig 1C

en: Data to Figure 1C

en: Fig 1B_1

en: Individual data to mean shown in Figure 1B

en: Code

media_type: m

en: Matlab code to read and plot the data

en: Fib 1B_3

en: Fig 1F_1

en: Individual data to mean shown in Figure 1F

en: Fig 1A

en: Data Figure 1A

en: Fig 1F_2

en: Fig 1B

en: Data in Figure 1B

en: Read Me

en: Description of the data tables

en: Fig 1B_2

en: Table 2

en: This table lists all NEXAFS data files in chronological order with PE carbon to oxygen signal intensity ratios -from which the atomic ratio were calculated in the paper - before ("preCtoO") and after ("postCtoO") each NEXAFS measurement. Also listed is the change in Na ("lossSodi"), O ("lossOxy"), Cl ("lossChlor"), and C ("lossCarb") signal intensity after the NEXAFS measurement compared to prior to the NEXAFS measurement.

en: Fig 1E

en: Data to Figure 1E

en: This table lists all data files in chronological order. "SampleTemp" refers to the reading of the PT-1000 at the side of the sample holder. "cellPressure" is the water vapour pressure during the measurements. From this, in presence of ice, the temperature of the ice sample can be calculated which is given in the column "iceTemp". "dT" is the difference, or temperature offset, between sensor's reading and the ice samples temperature. The offset is due to the sensor being mounted away from the cooled spot of the sample were it experiences heating from warmer parts of the sample holder. The off-set is used to calibrate the temperature sensor and the resulting temperature during the experiments is given in the column "temperature". "relHum" is the relative humidity above (supercooled) liquid and "concBrine" is the concentration of a NaCl solution in mol/l in equilibrium with ice at the experimental temperature. "Area" is the integrated PE signal.

en: Laboratory experiments are presented on the phase change at the surface of sodium chloride – water mixtures at temperatures between 259 K and 240 K. High selectivity to the upper few nanometres of the frozen solution – air interface is achieved by using electron yield near-edge X-ray absorption fine structure (NEXAFS) spectroscopy. We present the NEXAFS spectrum of the hydrohalite.

en: Data set on interfacial supercooling and the precipitation of hydrohalite in frozen NaCl solutions by X-ray absorption spectroscopy


en: species-distribution-model fagales species-range-map species-occurrence pinales species-richness

en: Occurrence maps for species of Fagales and Pinales with few records

en: Point_buffer.zip includes 267 occurrence maps of species that do not have enough occurrence data for polygon mapping.

en: Species range maps of species in Fagales and Pinales (with enough occurrences)

en: species_map.zip includes species 1690 range maps generated based on the integrated method described in Lyu et al., (2022). File names with (polygon) indicate that this map is only generated by polygon mapping, as there are not enough occurrences for SDMs.

en:
This database contains 1957 distribution maps of species from Fagales and Pinales constructed based on a method integrating polygon mapping and SDMs (Lyu et al., 2022).
To construct the maps, we first collected occurrence data from 48 different sources. According to the number of occurrences after data cleaning, three kinds of maps are constructed: (1) For species with more than 20 occurrences, we performed SDM and polygon mapping described in Lyu et al. (2022) and select the integration of the two layers as the distribution range; (2) For species with more than 4 but less than 20 occurrences, we only use polygon mapping to draw the distribution range; (3) For species with less than 4 occurrences, a 20-km buffer was generated around the occurrences as the distribution range. The maps were manually checked and evaluated (see Note S3 and Table S9 in Lyu et al., 2022 for details).

fagales

display_name: fagales

pinales

display_name: pinales

species-distribution-model

display_name: species-distribution-model

species-occurrence

display_name: species-occurrence

species-range-map

display_name: species-range-map

species-richness

display_name: species-richness

education

en: Education and science

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: Species distribution maps of Fagales and Pinales (GDPlants)


maintainer: Lisa Hülsmann

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

en: Calibration data

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

 Meta data
Reserve: Name of the forest reserve

Plot: Permanent plot number

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

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

dt: Length of the mortality period (years)

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

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

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

mDBH: Mean diameter at breast height (mm)

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

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

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

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

P: Mean annual precipitation sum (mm)

mT: Mean annual air temperature (°C)

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

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

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

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

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

empirical-mortality-models

display_name: empirical-mortality-models

forest-reserves

display_name: forest-reserves

inventory-data

display_name: inventory-data

tree-growth

display_name: tree-growth

tree-mortality

display_name: tree-mortality

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


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

en: Data plot of the forest station (NEB)

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

en: Site aerial photo (Neunkirch)

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

en: Site photo of the forest station (NEB)

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

en: Forest station data (NEB)

en: Data file.

en: Field station data (NEF)

en: Site photo of the field station (NEF)

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

en: Data plot of the field station (NEF)

en: High quality meteorological data are needed for long-term forest ecosystem research, particularly in the light of global change. The long-term data series published here comprises almost 20 years of measurements for two meteorological stations in Neunkirch in Switzerland where one station is located within a natural deciduous forest stand (NEB) with European beech (_Fagus sylvatica_; 160 yrs), sycamore maple (_Acer pseudoplatanus_; 160 yrs) and lime trees (_Tilia sp._; 110 yrs) as dominant tree species. A second station is situated in the very vicinity outside of the forest (field station, NEF). The meteorological time series are presented in hourly time resolution of air temperature, relative humidity, precipitation, photosynthetically active radiation (PAR) and wind speed. Neunkirch is part of the Long-term Forest Ecosystem Research Programme (LWF) established and maintained by the Swiss Federal Research Institute WSL.

climate-change

display_name: climate-change

long-term

display_name: long-term

meteo

display_name: meteo

meteorology

display_name: meteorology

par

display_name: par

precipitation

display_name: precipitation

relative-humidity

display_name: relative-humidity

swiss-forest-lab

display_name: swiss-forest-lab

temperature

display_name: temperature

wind-speed

display_name: wind-speed

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


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

en: Data plot of the field station (JUF)

en: Forest station data (JUB)

en: Site photo of the forest station (JUB)

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

en: Data plot of the forest station (JUB)

en: Site aerial photo (Jussy)

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

en: Site photo of the field station (JUF)

en: High quality meteorological data are needed for long-term forest ecosystem research, particularly in the light of global change. The long-term data series published here comprises almost 20 years of measurements for two meteorological stations in Jussy in Switzerland where one station is located within a natural broad-leaved forest stand (JUB) with sessile oak (_Quercus petrea_; 90 yrs), aspen (_Populus tremula_; 60 yrs) and European hornbeam (_Carpinus betulus_; 60 yrs) as dominant tree species. A second station is situated in the very vicinity outside of the forest (field station, JUF). The meteorological time series are presented in hourly time resolution of air temperature, relative humidity, precipitation, photosynthetically active radiation (PAR) and wind speed. Jussy is part of the Long-term Forest Ecosystem Research Programme (LWF) established and maintained by the Swiss Federal Research Institute WSL.

education

en: Education and science

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


en: soil-moisture precipitation discharge hydrology snowmelt climate-change

en: Shapefile of 307 catchments in Switzerland

en: Shapefile of the 307 medium-sized catchments in Switzerland. The "gridcode" provides the ID of the catchment used in the datafiles.

en: Daily simulated data for the reference period

en: Daily simulated discharge, precipitation, snowmelt, and soil moisture for the reference period 1981-2017 in mm.

en: Daily simulated data for the future period

en: Daily simulated discharge, precipitation, snowmelt, and soil moisture for the period 1981-2100 in mm for the 307 catchments.

en:
Daily discharge and the related hydro-meteorological variables precipitation, snowmelt, and soil moisture are provided for current (1981-2017) and for future climate conditions (1981-2100) for 307 medium-sized catchments in Switzerland. The catchments have a median catchment area of 117 km². The 307 catchments together form a set representative of the climatological conditions and runoff characteristics in Switzerland. The four variables were simulated at a daily resolution using the hydrological model PREVAH. PREVAH is a conceptual process-based model that was run in this study in its fully distributed version on a 500 m grid (Viviroli et al. 2009a). For the calibration, runoff time series from 140 mesoscale catchments covering the different runoff regimes were used. The model calibration was conducted over the period 1993-1997. Verification was performed on the period 1983-2005 using (i) volumetric deviation (Viviroli et al. 2007) and (ii) benchmark efficiency (Schäfli et al 2007) as objective functions. The calibration and validation procedures are described in detail in Köplin et al. (2010). The parameters for each model grid cell were derived by regionalizing the parameters obtained for the 140 catchments with a procedure based on ordinary kriging (Viviroli et al. 2009b, Köplin et al. 2010).
The calibrated and validated model was then driven with transient meteorological data (precipitation, temperature, radiation, and wind) representing both reference (1981-2017) and future climate conditions (2018-2099). The data were derived from the CH2018 climate scenarios (NCCS 2018) provided by the Swiss National Centre for Climate Services (NCCS). They were obtained from climate experiments produced with different climate modeling chains, consisting of a global and a regional circulation model each, within EUROCORDEX for three representative concentration pathways (RCP) emission scenarios. Downscaled output of ten climate model chains derived by quantile mapping were considered. The focus was on the chains of the EUR-11 domain with a horizontal resolution of 0.11 degrees (roughly 12.5 km). The climate model chains (GCM, RCM, RCP, and grid resolution) used are listed below:

- ICHEC-EC-EARTH	DMI-HIRHAM5	2.6	EUR-11
- ICHEC-EC-EARTH	DMI-HIRHAM5	4.5	EUR-11
- ICHEC-EC-EARTH	DMI-HIRHAM5	8.5	EUR-11
- ICHEC-EC-EARTH	SMHI-RCA4	2.6	EUR-11
- ICHEC-EC-EARTH	SMHI-RCA4	4.5	EUR-11
- ICHEC-EC-EARTH	SMHI-RCA4	8.5	EUR-11
- MOHC-HadGEM2-ES	SMHI-RCA4	4.5	EUR-11
- MOHC-HadGEM2-ES	SMHI-RCA4	8.5	EUR-11
- MPI-M-MPI-ESM-LR	SMHI-RCA4	4.5	EUR-11
- MPI-M-MPI-ESM-LR	SMHI-RCA4	8.5	EUR-11

*References*:

-	Köplin, N., D. Viviroli, B. Schädler, and R. Weingartner (2010), _How does climate change affect mesoscale catchments in Switzerland? - A framework for a comprehensive assessment_, Advances in Geosciences, 27, 111-119, doi:10.5194/adgeo-27-111-2010.
-	National Centre for Climate Services (2018), CH2018 - _Climate Scenarios for Switzerland_, Tech. rep., NCCS, Zurich.
-	Schäfli, B., and H. V. Gupta (2007), _Do Nash values have value?_, Hydrological Processes, 21, 2075-2080, doi:10.1002/hyp.6825.
-	Viviroli, D., J. Gurtz, and M. Zappa (2007), _The hydrological modelling system PREVAH. Part II - Physical model description_, Geographica Bernensia, 40, 1-89.
-	Viviroli, D., M. Zappa, J. Gurtz, and R. Weingartner (2009a), _An introduction to the hydrological modelling system PREVAH and its pre- and post-processing-tools_, Environmental Modelling & Software, 24, 1209-1222, doi:10.1016/j.envsoft.2009.04.001.
-	Viviroli, D., H. Mittelbach, J. Gurtz, and R. Weingartner (2009b), _Continuous simulation for flood estimation in ungauged mesoscale catchments of Switzerland-Part II: Parameter regionalisation and flood estimation results_, Journal of Hydrology, 377 (1), 208-225, doi:10.1016/j.jhydrol.2009.08.022.

discharge

display_name: discharge

hydrology

display_name: hydrology

snowmelt

display_name: snowmelt

soil-moisture

display_name: soil-moisture

en: Simulated future discharge and climatological variables for medium-sized catchments in Switzerland


maintainer: Varun Sharma

en: snow-atmosphere-interaction mesoscale-modelling alps blowing-snow antarctica

en: REPRODUCIBILITY_SIMULATION.zip contains all the extraneous files required to perform the simulations in associated manuscript (see Citations 3 in README.txt). The purpose of sharing these files apart from purposes of reproducibility is to also serve as templates for users to learn the workflow of CRYOWRF and perform simulations for their own purposes.

en:
REPRODUCIBILITY_POSTPROCESSING.zip contains data and scripts used to produce all figures from for the associated manuscript submitted for peer review ( see section on Citations below )

The folders stand for the three case studies presented in the manuscript. Two case studies (case Ia and case Ib) are on simulations in Antarctica and one case study
case II is for simulations in the Alps.

The associated data in the form of netcdf files or text files were produced using CRYOWRF v1.0

Apart from reproducibility, the intention of sharing these scripts is also to make it easy for new users to adopt CRYOWRF and be efficient, in particular in processing snowpack outputs.

The scripts were tested on multiple machines (different OSes) with the attached YAML file (wrf_analysis.yml) to setup the conda environment. All scripts were run using spyder as the IDE.

en:
This repository contains data required for reproducibility of the results to be published in the associated manuscript.

Apart from reproducibility, the attached datasets also serve as templates for new users to adopt CRYOWRF in their research.

The datasets consist of two folders organized in zip format:

1. REPRODUCIBILITY_SIMULATION:
  Consists of namelists for WPS, WRF and SNOWPACK to reproduce simulations published in the manuscript
  Additional files include datasets (from IMAU-FDM / RACMO, see "credits" below ) as well as helper python scripts to
  produce *.sno files
  which are used as initial conditions for SNOWPACK in CRYOWRF.

2. REPRODUCIBILITY_POSTPROCESSING:
   Includes outputs of CRYOWRF and python scripts used to prepare figures in the manuscript.

Each of the folders have their own readme files for more details.

 Code
citation: Varun Sharma. (2021, July 2). vsharma-next/CRYOWRF: CRYOWRF v1.0 (Version v1.0). Zenodo. http://doi.org/10.5281/zenodo.5060165

location: https://gitlabext.wsl.ch/atmospheric-models/CRYOWRF   (stable releases / institutional repo)
        https://github.com/vsharma-next/CRYOWRF            (dev branches / developer repo)

 Publication
**Introducing CRYOWRF v1.0: Multiscale atmospheric flow simulations with advanced snow cover modelling.**
Varun Sharma, Fraziska Gerber and Michael Lehning, Submitted to Geoscientific Model Development

 Acknowledgements
We thank Peter Kuipers Munneke (P.KuipersMunneke@uu.nl) for preparing and sharing outputs of IMAU-FDM and RACMO used for initial conditions for case Ia. The relevant citations for the methods through which these datasets were generated are:

* Kuipers Munneke, P., S. R. M. Ligtenberg, B. P. Y. Noël, I. M. Howat, J. E. Box, E. Mosley-Thompson, J. R. McConnell, K. Steffen, J. T. Harper, S. B. Das and M. R. van den Broeke. 2015. Elevation change of the Greenland ice sheet due to surface mass balance and firn processes, 1960-2014. The Cryosphere, 9, 2009-2025. doi:10.5194/tc-9-2009-2015

 * Ligtenberg, S. R. M., P. Kuipers Munneke, B. P. Y. Noël, and M. R. van den Broeke. 2018. Brief communication: Improved simulation of the present-day Greenland firn layer (1960-2016). The Cryosphere, 12, doi:10.5194/tc-12-1643-2018

alps

display_name: alps

antarctica

display_name: antarctica

blowing-snow

display_name: blowing-snow

mesoscale-modelling

display_name: mesoscale-modelling

snow-atmosphere-interaction

display_name: snow-atmosphere-interaction

en: Reproducibility Dataset for CRYOWRF v1.0