en: perception-of-ecosystem-services nfi-photos adults-and-teenagers online-questionnaire-survey visual-attractiveness

en: Questionnaire Italian

en: Questionnaire French

en: Dataset in csv-format

en: SPSS-Dataset

en: Codebook to SPSS-file

en: Questionnaire German

en: This questionnaire survey was conducted as an online survey and aimed at investigating the relationship between physical forest characteristics, visual attractiveness of forest and the perception of ecological and cultural ecosystem services in urban forests. Each participant was shown 6 photos out of a pool of 50 photos taken from the Swiss National Forest Inventory (NFI) database. Physical forest characteristics were derived from the photos. The study was conducted as part of the "WaMos meets LFI" (WML) project.

adults-and-teenagers

display_name: adults-and-teenagers

nfi-photos

display_name: nfi-photos

online-questionnaire-survey

display_name: online-questionnaire-survey

perception-of-ecosystem-services

display_name: perception-of-ecosystem-services

visual-attractiveness

display_name: visual-attractiveness

educ

en: Education, culture and sport

envidat

en: EnviDat: the Environmental Data Portal

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

en: Relationship between physical forest characteristics, visual attractiveness and perception of ecosystem services in urban forests


maintainer: EnviDat

en: metadata-convention research-data-management meteorological-data-format csv nead

state: active

type: dataset

en: MeteoIO (future reference implementation)

media_type: text/html

format: HTML

mimetype: text/html

en: PyNEAD (future reference implementation)

format: SERVICE

en: NEAD syntax v0.1 (EBNF)

media_type: text/plain

format: TXT

mimetype: text/plain

en: NEAD on GitHub

en:
Acknowledgement: The NEAD format includes NetCDF metadata and is proudly inspired by both SMET and NetCDF formats. NEAD is designed as a long-term data preservation and exchange format.

The NEAD specifications were presented at the "WMO Data Conference 2020 - Earth System Data Exchange in the 21st Century" (Virtual Conference).

-----------------------

Summary:
The Non-Binary Environmental Data Archive (NEAD) format is being developed as a generic and intuitive format that combines the self-documenting features of NetCDF with human readable and writeable features of CSV. It is designed for exchange and preservation of time series data in environmental data repositories.

License: The NEAD specifications are released to the public domain under a Creative Commons CC0 "No Rights Reserved" international license. You can reuse the information contained herein in any way you want, for any purposes and without restrictions.

csv

display_name: csv

metadata-convention

display_name: metadata-convention

meteorological-data-format

display_name: meteorological-data-format

nead

display_name: nead

research-data-management

display_name: research-data-management

educ

fr: Éducation, culture et sport

de: Bildung, Kultur und Sport

it: Istruzione, cultura e sport

fr: EnviDat: le portail de données environnementales

de: EnviDat: das Umwelt-Datenportal

it: EnviDat: il portale dei dati ambientali

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

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

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

political_level: other

wsl

capacity: public

type: organization

approval_status: approved

key: guid

key: uri

value: Envidat Harvester

en: Non-Binary Environmental Archive Data (NEAD) format


en: flora-change zurich occurrence uetliberg plant-species

media_type: text/csv

en:
The list gives the clearly identifiable plant species from Schinz (1775). Die Reise auf den Uetliberg. Verlag des Waysenhauses, Zürich). Several species given in Schinz (1775) are not identifiable to the species level and are not included in the list. Similarly, Vicia pisiformis, Erbsenartige Wicke, given by Schinz (1775) is probably a misidentification and also not included in the list.

Latin plant species name Schinz 1775: Latin plant name (if) given by Schinz (1775); na: not available
German plant species name Schinz 1775: German plant name given by Schinz (1775)
Latin plant species name Info Flora 2024: Latin plant name according to www.infoflora.ch in 2024
German plant species name Info Flora 2024: German plant name according to www.infoflora.ch in 2024
Plant species still occurring in 2020: Plant species given in Schinz (1775) still occurring at the Uetliberg in 2020 (Zürcherische Botanische Gesellschaft. 2020. Flora des Kanton Zürich. Haupt, Bern); occurrence of Thesium alpinum, Alpen-Bergflachs, according to floristic knowledge of Rolf Holderegger and Michèle Büttner; 1: still occurring; 0: no longer occurring / extinct.

format: CSV

en:
The list gives the clearly identifiable plant species from Schinz (1775). Die Reise auf den Uetliberg. Verlag des Waysenhauses, Zürich). Several species given in Schinz (1775) are not identifiable to the species level and are not included in the list. Similarly, *Vicia pisiformis*, Erbsenartige Wicke, given by Schinz (1775) is probably a misidentification and also not included in the list.
Latin plant species name Schinz 1775: Latin plant name (if) given by Schinz (1775); na: not available
German plant species name Schinz 1775: German plant name given by Schinz (1775)
Latin plant species name Info Flora 2024: Latin plant name according to www.infoflora.ch in 2024
German plant species name Info Flora 2024: German plant name according to www.infoflora.ch in 2024
Plant species still occurring in 2020: Plant species given in Schinz (1775) still occurring at the Uetliberg in 2020 (Zürcherische Botanische Gesellschaft. 2020. Flora des Kanton Zürich. Haupt, Bern); occurrence of *Thesium alpinum*, Alpen-Bergflachs, according to floristic knowledge of Rolf Holderegger and Michèle Büttner; 1: still occurring; 0: no longer occurring / extinct.

flora-change

display_name: flora-change

occurrence

display_name: occurrence

plant-species

display_name: plant-species

uetliberg

display_name: uetliberg

zurich

display_name: zurich

en: Plant species list from 1775 and 2020 for Uetliberg Zürich


en: qpcr field-based-protocol threatened-species crispr-dx edna biodiversity-monitoring african-manatee crispr-cas environmental-dna

en: Description of project and folders and files

media_type: application/zip

en: File containing overview of site names and extract number (field-based or lab-based extraction). The extract_number_field_based corresponds to the identically called column in CRISPR_field_based_classifications.csv file in the data folder, as the extract_number_lab_based to the column in the file CRISPR_lab_based_classifications.csv file and the qPCR_Cp_2nd_derivative.csv file (also in the data folder). The file includes the GPS coordinates of the sampling location (transect start point).

format: ZIP

en:
Folder containing the data files with Cp values (qPCR) and the CRISPR-Dx classifications. CRISPR_field_based_classifications.csv file contains the classifications per pool per extract (0: no detection, 1: detection) for the African manatee (Trichechus senegalensis).
CRISPR_lab_based_classifications.csv file contains the classifications per pool per extract (0: no detection, 1: detection).
qPCR_Cp_2nd_derivative.csv file contains the Cp value of the 8 replicates of each extract.

en:
Data associated to the publication "Rapid field-based detection of a threatened and elusive species with environmental DNA and CRISPR-Dx"

 Authors:

Flurin Leugger, Martina Lüthi, Michel Schmidlin, Zacharias Kontarakis and Loïc Pellissier

 Contact:

flurinleugger@gmail.com
loic.pellissier@usys.ethz.ch

 Project description:

We collected eDNA samples in the Conkouati-Douli National Park in the Republic of Congo in 2023 in collaboration with Beauval Nature and HELP Congo. We analyzed the samples on site in the national park using CRISPR-Dx assays to detect the African manatee (*Trichechus senegalensis*). Additionally, we transported the remaining samples (buffer) to Switzerland and used a high-sensitivity protocol with CRISPR-Dx assays and a qPCR assay to verify the field-based detections. The qPCR of Hunter et al. (2018) detects the genus manatee (Trichechus). See publication for more details (doi will be added after publication).

 Folders:

 lateral_flow_tests_images\:

Images of the lateral flow tests used to analyze the eDNA extracts in the national park. File names correspond to the site names. At each site, we took two filter replicates. We ran 8 PCRs per filter/extract and pooled two PCRs together, resulting in 4 CRISPR-Dx assays per extract. The EVE number on top of the tests indicates the environmental extract number we use to track the extracts in our data base. It corresponds to the extract_number_field_based in the metadata and data folder. The negative extraction control with the strongest "band" was placed right to the eDNA extract on each image (labelled hand written with NC x.y).

 metadata\:

File containing overview of site names and extract number (field-based or lab-based extraction). The extract_number_field_based corresponds to the identically called column in CRISPR_field_based_classifications.csv file, as the extract_number_lab_based to the column in the file CRISPR_lab_based_classifications.csv file and the qPCR_Cp_2nd_derivative.csv file. The file includes the GPS coordinates of the sampling location (transect start point).

 data\:

Folder containing the files with Cp values (qPCR) and the CRISPR-Dx classifications. CRISPR_field_based_classifications.csv file contains the classifications per pool per extract (0: no detection, 1: detection) for the African manatee (Trichechus senegalensis).
CRISPR_lab_based_classifications.csv file contains the classifications per pool per extract (0: no detection, 1: detection).
qPCR_Cp_2nd_derivative.csv file contains the Cp value of the 8 replicates of each extract.

african-manatee

display_name: african-manatee

biodiversity-monitoring

display_name: biodiversity-monitoring

crispr-cas

display_name: crispr-cas

crispr-dx

display_name: crispr-dx

edna

display_name: edna

environmental-dna

display_name: environmental-dna

field-based-protocol

display_name: field-based-protocol

qpcr

display_name: qpcr

threatened-species

display_name: threatened-species

en: Field-based eDNA analysis to detect the threatened and elusive African manatee


maintainer: Anita Risch

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

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)

format: XLS

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

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

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

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

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

#References

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

ecosystem-coupling

display_name: ecosystem-coupling

ecosystem-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

educ

en: Education, culture and sport

envidat

en: EnviDat: the Environmental Data Portal

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

en: Ecosystem coupling and multifunctionality - exclosure experiment


data-set-on-snow-instability

maintainer: EnviDat Support

title_for_slug: data-set-on-snow-instability

en: weak-layer slab snow-stability-evaluation slab-tensile-support failure-initiation snow-avalanche rutschblock propgatoin-saw-test crack-propagation avalanche-forcasting

en: data set on snow instability

mimetype: text/csv

en: Read-me file on snow instability data

media_type: application/pdf

format: PDF

mimetype: application/pdf

en:
These data on snow instability include three data subsets that were analyzed and the results published by Reuter and Schweizer (2018) who suggest a novel framework on how to describe snow instability by failure initiation, crack propagation and slab tensile support.

Please refer to the Read-me file for further details on the data.

These data are the basis of the following publication:
Reuter, B. and Schweizer, J., 2018. Describing snow instability by failure initiation, crack propagation and slab tensile support. Geophys. Res. Lett., 45, doi: 10.1029/2018GL078069.

avalanche-forcasting

display_name: avalanche-forcasting

crack-propagation

display_name: crack-propagation

failure-initiation

display_name: failure-initiation

propgatoin-saw-test

display_name: propgatoin-saw-test

rutschblock

display_name: rutschblock

slab

display_name: slab

slab-tensile-support

display_name: slab-tensile-support

snow-avalanche

display_name: snow-avalanche

snow-stability-evaluation

display_name: snow-stability-evaluation

weak-layer

display_name: weak-layer

en: Data set on snow instability


en: hill dust snow turbulence deposition particles atmosphere

en: preferential deposition patterns of all simulations performed

en: The data consist of matlab files. Each files contains a 2D array with the values of deposition at the surface nodes. Each array has Nx x Ny values. Please refer to the original paper for additional information on the spatial resolution and grid size.

mimetype: application/zip

en:
Preferential deposition of snow and dust over complex terrain is responsible for a wide range of environmental processes, and accounts for a significant source of uncertainty in surface mass balances of cold and arid regions. Despite the growing body of literature on the subject, previous studies reported contradictory results on the location and magnitude of deposition maxima and minima. This study aims at unraveling the governing processes of preferential deposition in neutrally stable atmosphere and to reconcile seemingly inconsistent results of previous works. For this purpose, a comprehensive modeling approach is developed, based on large eddy simulations of the turbulent airflow, Lagrangian stochastic model of particle trajectories, and immersed-boundary method to represent the underlying topography. The model performance is tested against wind tunnel measurements of dust deposition around isolated and sequential hills. A scale analysis is then performed to investigate the dependence of snowfall deposition on the particle Froude and Stokes numbers, which fully account for the governing processes of inertia, flow advection, and gravity. Additional simulations are performed, to test whether the often used assumption of inertialess particles yields accurate deposition patterns. We finally show that our scale analysis provides qualitatively similar results for hills with different aspect ratios.

This dataset contains the results of the LES-LSM model. Each Matlab file contains a 2D array of deposition values (in kg/m2) in each surface node (ix, iy) of the Cartesian grid. The file names are consistent with the simulation numbers listed in the original paper. For additional information, please refer to "Preferential deposition of snow and dust over hills: governing processes and relevant scales" by F. Comola, M. G. Giometto, S. T. Salesky, M. B. Parlange, and M. Lehning, Journal of Geophysical Research: Atmospheres, 2019.

atmosphere

display_name: atmosphere

deposition

display_name: deposition

dust

display_name: dust

hill

display_name: hill

particles

display_name: particles

snow

display_name: snow

turbulence

display_name: turbulence


en: channel drainage-network dynamics catchment catchment-data water-level drainage precipitation

en: Documentation for the Short-term Drainage Density Dynamics Dataset for the Haute-Mentue Catchment (dataset_of_flowing_drainage_network_lengths_water_levels_and_precipitation_for_the_haute-mentue_catchment.csv). This document provides a detailed description of the collected data, the locations where it was recorded, the data format, and the curation process applied.

en: The dataset consists of time series of measured surface and groundwater levels, calculated flowing drainage network lengths, and nearby precipitation data for two sub-catchments of the Haute-Mentue catchment, Switzerland (Summer-Autumn 2022). The details of the dataset are described in the provided documentation (short-term_drainage_density_dynamics_dataset_documentation_for_the_haute-mentue_catchment.pdf)

en: The dataset contains time series of water levels, precipitation measured in the two sub-catchments of the Haute-Mentue catchment and its vicinity during summer and autumn 2022, as well as flowing drainage network lengths calculated for these areas using the CEASE method developed by the authors. Detailed description of the dataset is provided in the documentation.

catchment

display_name: catchment

catchment-data

display_name: catchment-data

channel

display_name: channel

drainage

display_name: drainage

drainage-network

display_name: drainage-network

dynamics

display_name: dynamics

precipitation

display_name: precipitation

water-level

display_name: water-level


maintainer: Marco Moretti

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

en: Taxonomic and functional metrics in the community plots

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

en: Deprecated-Predictors

en:
The compress file includes the rster files of the predictors used in the analyses, including the climate, resource availability, land-use and beekeeping intensity metrics.

The raster on the climate contains the PCA axes on the CHELSA variables.
The raster on resource availability contains the PCA axes on plant communities
The raster on land-use contains the land-use composition at 2500 m.
The raster on beekeeping intensity contains thedensity of hives within 2500 m

en: Protected areas

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

en: Elevation and waterbodies

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

en: Variable importance, model evaluation, partial dependence plots

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

en: Wild bee trait data

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

en: Spatial environmental predictors and responses

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

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

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

anthophila

display_name: anthophila

beta-diversity

display_name: beta-diversity

biodiversity

display_name: biodiversity

climate

display_name: climate

community-indices

display_name: community-indices

elevation-gradient

display_name: elevation-gradient

functional-diversity

display_name: functional-diversity

hymenoptera

display_name: hymenoptera

predictive-modelling

display_name: predictive-modelling

protected-areas

display_name: protected-areas

resource-availability

display_name: resource-availability

switzerland

display_name: switzerland

urbanization

display_name: urbanization

wild-bee

display_name: wild-bee

educ

en: Education, culture and sport

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


en: geoinformation-system raster-processing digital-planning qgis-plugin seilaplan cable-yarding open-source geodata-processing swiss-geodata digital-elevation-model

en: View video on youtube!

en: DHM-Kacheln zusammenfügen

en:
In order to use the QGIS plugin ‘Seilaplan’ for digital cable line planning, a digital terrain model (DTM) is required. In this tutorial video, we show how to merge multiple DTM raster tiles into one file, using the QGIS tool ‘Virtual Raster’. This simplifies the digital planning of a cable line using the QGIS plugin ‘Seilaplan’. Please note that the tutorial language is German!

Link to Seilaplan website: https://seilaplan.wsl.ch

***************************

Für die Verwendung des QGIS Plugins Seilaplan zur digitalen Seillinienplanung ist ein digitales Höhenmodell (DHM) nötig. In diesem Tutorialvideo zeigen wir, wie man mit dem QGIS-Plugin Virtuelles Raster mehrere DHM-Kacheln zu einem einzigen Rasterfile zusammenfügen und abspeichern kann. Für die Seillinienplanung mit Seilaplan muss nun nur noch eine Datei, mein neues virtuelles Raster, ausgewählt werden.

Link zur Seilaplan-Website: https://seilaplan.wsl.ch

cable-yarding

display_name: cable-yarding

digital-elevation-model

display_name: digital-elevation-model

digital-planning

display_name: digital-planning

geodata-processing

display_name: geodata-processing

geoinformation-system

display_name: geoinformation-system

open-source

display_name: open-source

qgis-plugin

display_name: qgis-plugin

raster-processing

display_name: raster-processing

seilaplan

display_name: seilaplan

swiss-geodata

display_name: swiss-geodata

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: Seilaplan Tutorial: Merge DTM tiles


maintainer: Giulia Francesca Azzurra Donati

en: ecological-corridors ecosystem-services urban-planning biodiversity circuit-theory network-analysis

en: Amphibian movement resistance layers and scripts for connectivity modeling - part 1

en: The zipped folder includes the script to aggregate the resistance layers into squared and hexagonal grids. The subfolders “Boundaries”, “Layers”, “Reference_grids”, and “Resistance_from_SDMs” contain files either called by the code or created in the process.The subfolder “Inputs_for_Circuitscape” contains the inputs to run Circuitscape, after doing some subsequent processing steps in QGIS (listed in the R script) with the files created with the script.

en: Amphibian movement resistance layers and scripts for connectivity modelling - part 2

en: The zipped folder includes the script to create and analyse the networks from Circuitscape outputs. The subfolders “Boundaries”, “Layers”, and “Reference_net” contain files either called by the code or created in the process. The subfolder “Outputs_from_Circuitscape” contains the outputs from Circuitscape including node and branch cumulative currents in a network format.

en: This data includes (1) Scripts to aggregate landscape resistance layers into squared and hexagonal grids (i.e., different representations and resolutions), (2) Input resistance layers and focal nodes in .txt format to run in Circuitscape (Python implementation v4.0.5). Circuitscape is a software tool for modeling and analyzing landscape connectivity, which simulates movement of organisms across landscapes by estimating resistance to movement across each point of the landscape. (3) Scripts for the ecological network analysis, and (4) environmental predictors for amphibian whole-life cycle habitats used to describe the local environment for BGI design (i.e. topographic, hydrologic, edaphic, vegetation, land-use derived, movement-ecology related).

biodiversity

display_name: biodiversity

circuit-theory

display_name: circuit-theory

ecological-corridors

display_name: ecological-corridors

ecosystem-services

display_name: ecosystem-services

network-analysis

display_name: network-analysis

urban-planning

display_name: urban-planning

en: Multi-Scale Prioritization framework for Urban Blue-Green Infrastructure Planning to Support Biodiversity: Data & Codes


en: pollen-metabarcoding bumblebees zurich basel bombus-pasquorum bern bees bombus-lapidarius urban macronutrients foraging-behaviour lad-use-chages nutrient-intake dietary-patterns rural

en:
Processed data. The dataset contains the functional diversity metrics based on the plant composition from the leg-baskets per bumblebee individual. It contains:
- SampleID: Combining bumblebee ID, location, landscape and replica
- Location: canton, levels: Bern =BE; Basel = BS; Zurich =ZH
- Landscape: landscape type, levels: Urban = U; Rural = R
- Replicate: sampling place (800-m buffer) within location and landscape. Levels: A-E.
- LocationLandscape: combining location and landscape
- Bumblebee_species: the two studied species, levels: B.pasquorum; B. lapidarius
- Fric.w: Weighted functional richness
-Fric: functional richness
-FEve.w: Weighted functional evenness
- FEve: functional evenness
- FDiv.w: weighted functional divergence
- FDiv: functional divergence

en:
The dataset contains the amino acid content and ratios for the two bumblebees. Measures are taken only from pollen from the leg-baskets. SampleID is not the same as in the metabarcoding, several samples from different bumblebees were merged within a Location ,Landscape and Replica. Not for all the samples there is information on both amino acids and fatty acids. The columns are:
- SampleID_chemical: The ID for chemical analyses
- Location: the three Swiss cantons studied. Levels: Bern =BE; Basel = BS; Zurich =ZH
- Landscape: the two typea of human-dominated ecosystems, nested to the Swiss canton. Levels: Urban = U; Rural = R
- Replicate: sampling place (800-m buffer) nested with the location and the landscape. Levels: A-E.
- Bumblebee_species: the two studied species, levels: B.pasquorum; B. lapidarius
- LocationLandscape: Combining location and landscape
- Asp, Thr, ..., Arg: Content of individual amino acids. Amino acids are written as abbreviated names. FUll names be checked here: https://en.wikipedia.org/wiki/Amino_acid
- sum: total sum of amino acid content (mg)
- sumessential: total sum essential amino acids (mg)
-sumnon-essential: total sum non-essential amino acids (mg)
- proportionnonessentialessential: proportion between essential and non-essential amino acids.

en:
The dataset contains the information on the 16 study sites:
- Location: the three Swiss cantons studied. Levels: Bern =BE; Basel = BS; Zurich =ZH
- Landscape: the two typea of human-dominated ecosystems, nested to the Swiss canton. Levels: Urban = U; Rural = R
- Replicate: sampling place (800-m buffer) nested with the location and the landscape. Levels: A-E.
- Site_ID: combination of location, landscape and replicate
- X: X coordinate, WGS84
- Y: Y coordinate WGS84
- Plant S in landscape: Plant species richness within the 800 m calculated using both information from the Global Biodiversity Information. Facility (GBIF) and InfoFlora (www.infoflora.ch).
- % Buildings: the proportion of buildings and other impervious surfaces within 800 m radius.
- % Agricultural: the proportion of agricultural land and other impervious surfaces within 800 m radius.
- % Water: the proportion of water and other impervious surfaces within 800 m radius.
- % Meadows & grasslands: the proportion of meadows and grasslands and other impervious surfaces within 800 m radius.
The raw metabarcoding data is archived in NCBI project PRJNA1137320.

en:
The dataset contains the fatty acid content and ratios for the two bumblebees. Measures are taken only from pollen from the leg-baskets. SampleID is not the same as in the metabarcoding, several samples from different bumblebees were merged within a Location ,Landscape and Replica. Not for all the samples there is information on both amino acids and fatty acids. The columns are:
- SampleID_chemical: The ID for chemical analyses
- Location: the three Swiss cantons studied. Levels: Bern =BE; Basel = BS; Zurich =ZH
- Landscape: the two typea of human-dominated ecosystems, nested to the Swiss canton. Levels: Urban = U; Rural = R
- Replicate: sampling place (800-m buffer) nested with the location and the landscape. Levels: A-E.
- Bumblebee_species: the two studied species, levels: B.pasquorum; B. lapidarius
- LocationLandscape: combination between location and landscape
- Caprylic, Pelargonic, ..., Lacceroic: Content of individual fatty acids acids.
- sum: total sum of fatty acid content (mg)
- unsaturatedsum: total sum unsaturated fatty acids (mg)
- saturatedsum: total sum saturated fatty acids (mg)
- omega3sum: total sum Omega 3 fatty acids (mg)
- omega6sum: total sum Omega 6 fatty acids (mg)
- omega9sum: total sum Omega 9 fatty acids (mg)
- omega6to3ratio: ratio Omega 6 to Omega3 fatty acids
-saturatedtounsaturatedration: ratio between saturated and unsaturated fatty acids

en:
Processed data. The dataset contains the plant species richness in the leg-baskets per bumblebee individual. It contains:
- SampleID: Combining bumblebee ID, location, landscape and replica
- Location: canton, levels: Bern =BE; Basel = BS; Zurich =ZH
- Landscape: landscape type, levels: Urban = U; Rural = R
- Replicate: sampling place (800-m buffer) within location and landscape. Levels: A-E.
- LocationLandscape: combining location and landscape
- Bumblebee_species: the two studied species, levels: B.pasquorum; B. lapidarius
- Plant species richness: the number of plant species found in the pollen of the leg-baskets.

en:
Processed data. The dataset contains the phylogeneitc diversity metrics based on the plant composition from the leg-baskets per bumblebee individual. It contains:
- SampleID: Combining bumblebee ID, location, landscape and replica
- Location: canton, levels: Bern =BE; Basel = BS; Zurich =ZH
- Landscape: landscape type, levels: Urban = U; Rural = R
- Replicate: sampling place (800-m buffer) within location and landscape. Levels: A-E.
- LocationLandscape: combining location and landscape
- Bumblebee_species: the two studied species, levels: B.pasquorum; B. lapidarius
- PVar: phylogenetic variance
- PRic: Phylogenetic richness
- PEve: Phylogenetic evenness
- PClu: Phylogenetic clustering

en:
The dataset contains the plant trait values obtined from published sources. It contains:
- Kingddom: taxonomic
- Phylum: taxonomic
- Order: taxonomic
- Family: taxonomic
- Genus: taxonomic
- Species: species name
- plant.species: full scientific name
- native_exotic: origin status. As presented in https://www.doi.org/10.16904/envidat.210
- pollination mode: vector of pollination. As presented in https://www.doi.org/10.16904/envidat.210
- Flowering_months_duration: Number of flowering months. As presented in https://www.doi.org/10.16904/envidat.210
- start_flowering: month of the starting of the flowering. As presented in https://www.doi.org/10.16904/envidat.210
- growth_form_category: plant growth form. As presented in https://www.doi.org/10.16904/envidat.210
- plant-height: plant heght in meters. As presented in https://www.doi.org/10.16904/envidat.210
- inflorescence: Logic, plant with single flowers (0) or inflorescences (1). As presented in https://www.doi.org/10.16904/envidat.210
- structural_blossom_class: depicting the accessibility of the flowers. As presented in https://www.doi.org/10.16904/envidat.210
- symmetry: floral symmetry. As presented in https://www.doi.org/10.16904/envidat.210
- nectar: logic, nectar present. As presented in https://www.doi.org/10.16904/envidat.210
- pollen: logic, pollen rewards present. As presented in https://www.doi.org/10.16904/envidat.210
- oil: logic. oil present. As presented in https://www.doi.org/10.16904/envidat.210
- sugar.concentration: the amount of sugar present in the nectar, in mg.
Additional information can be found in https://doi.org/10.1016/j.dib.2021.107243

en:
The dataset contains the filtered plant composition1 (removing species with too low relative abundances) and the relative abundance obtained from DNA metabarcoding on pollen samples for both the leg-baskets and the body. The dataset contains the following columns:
- SampleID: Combining bumblebee ID, location, landscape and replica
- Abundance: numeric, relative abundance
- BumblebeeID: numerical ID for each bumblebee individual within a location, landscape and replicate sampling place.
- Location: canton, levels: Bern =BE; Basel = BS; Zurich =ZH
- Landscape: landscape type, levels: Urban = U; Rural = R
- Replicate: sampling place (800-m buffer) within location and landscape. Levels: A-E.
- LocationLandscape:
- Bumblebee_species: the two studied species, levels: B.pasquorum; B. lapidarius
- Transportation_structure: bumblebee pollen transportation structure, levels: B = Body; L = leg-baskets (i.e. corbicula)
- Kingddom: taxonomic
- Phylum: taxonomic
- Order: taxonomic
- Family: taxonomic
- Genus: taxonomic
- Species: plant sicentific name
-Binomial_abundance: Logic, indicating if the plant species is included (1).
The raw metabarcoding data is archived in NCBI project PRJNA1137320

en:
Data on the diet of urban and rural bumblebees individuals, Bombus lapidarius and Bombus pascuorum, collected in Switzerland (cantons Bern, Basel and Zürich) obtained using metabarconding and chemical analyses from two pollen transportation structures, that is, the body and the leg-baskets (i.e., corbicula). The bumblebees were collected by Egenberger et al., 2019 (https://doi.org/10.5061/dryad.qt8mr4v)
The data contains:
- The composition and relartive abundance of plant species in the body and the leg-baskets, separately.
- The content and ratios of two groups of macronutrients, that is, amino acids and fatty acids.
The dataset contains the data used in the paper "Urban bumblebees diversify their foraging strategy to maintain nutrient intake" as well as unpublished data.

basel

display_name: basel

bees

display_name: bees

bern

display_name: bern

bombus-lapidarius

display_name: bombus-lapidarius

bombus-pasquorum

display_name: bombus-pasquorum

bumblebees

display_name: bumblebees

dietary-patterns

display_name: dietary-patterns

foraging-behaviour

display_name: foraging-behaviour

lad-use-chages

display_name: lad-use-chages

macronutrients

display_name: macronutrients

nutrient-intake

display_name: nutrient-intake

pollen-metabarcoding

display_name: pollen-metabarcoding

rural

display_name: rural

urban

display_name: urban

zurich

display_name: zurich


maintainer: Lisa Hülsmann

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

en: German data

en:
READ ME for

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

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

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

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

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

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

en: Swiss data reduced

en: Ukrainian data

en: Swiss data full

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

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

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

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

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

fagus-sylvatica

display_name: fagus-sylvatica

forest-inventory

display_name: forest-inventory

forest-reserves

display_name: forest-reserves

mortality-models

display_name: mortality-models

primeval-forests

display_name: primeval-forests

tree-mortality

display_name: tree-mortality

educ

en: Education, culture and sport

envidat

en: EnviDat: the Environmental Data Portal

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

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


disdrometer-data-gotschnagrat

title_for_slug: disdrometer-data-gotschnagrat

en: disdrometer raclets visibility precipitation hydrometeors

en: Disdrometer Data Gotschnagrat

en: The zip folder contains one netCDF file per day for Gotschnagrat from February 11 to March 27 2019 with a temporal resolution of 30 seconds (time in UTC). The naming convention for the files is Gotschna_YYYYMMDD.nc and the files include the following: characteristics of hydrometeors (e.g. diameter, fall velocity, amount per diameter class,...), precipitation rate, radar reflectivity, visibility range, weather codes and instrument performance.

en: A laser optical disdrometer (Parsivel² , OTT Hydromet) was deployed at Gotschnagrat (LON: 9.849, LAT: 46.859) to measure hydrometeors by extinction when passing a laser beam. The instrument can classify eight different kinds of precipitation, including rain, hail, snow, drizzle, and hybrid forms. The dataset contains information on precipitation amount and type for the period of February 11 to March 27 2019 at Gotschnagrat.

disdrometer

display_name: disdrometer

hydrometeors

display_name: hydrometeors

precipitation

display_name: precipitation

raclets

display_name: raclets

visibility

display_name: visibility


rorcc

maintainer: Tobias Wechsler

title_for_slug: rorcc

en: run-of-river-power-plants design-discharge climate-change hydropower environmental-flow

en: RoRCC

en:
The dataset “RoRCC” consists of simulation-based results on climate change impacts on Alpine RoR power production; it is based on 21 Swiss RoR power plants, with a total production of 5.9 TWh a-1. The dataset contains the following information:
-	metadata on the RoR power plants under consideration
-	annual and seasonal production scenarios differentiated into three emission scenarios (RCP2.6, RCP4.5, RCP8.5) and three future periods (T1: 2020–2049, T2: 2045–2074, T3: 2070–2099)
-	annual and seasonal production loss due to environmental flow requirements
-	annual and seasonal the technical increase potential (via design discharge optimisation)
-	annual and seasonal changes in the hydrological cycle for the three emission scenarios (RCP2.6, RCP4.5, RCP8.5) and three future periods (T1: 2020–2049, T2: 2045–2074, T3: 2070–2099)

en:
The dataset "RoRCC" consists of simulation-based results on climate change impacts on Alpine RoR power production; it is based on 21 Swiss RoR power plants, with a total production of 5.9 TWh a-1. The dataset contains the following information:
1) metadata on the RoR power plants under consideration, 2) annual and seasonal production potential scenarios under into three emission scenarios (RCP2.6, RCP4.5, RCP8.5) and three future periods (T1: 2020–2049, T2: 2045–2074, T3: 2070–2099), 3) annual and seasonal streamflow scenarios, 4) annual and seasonal production loss due to environmental flow requirements, 5) annual and seasonal the technical increase potential (via design discharge optimisation) and 6) annual and seasonal changes in the hydrological cycle.

climate-change

display_name: climate-change

design-discharge

display_name: design-discharge

environmental-flow

display_name: environmental-flow

hydropower

display_name: hydropower

run-of-river-power-plants

display_name: run-of-river-power-plants


maintainer: Yves Bühler

en: wingtra snow-depth-mapping drone-data uav photogrammetry orthophoto dsm

en: Data Access

en:
- DSM (10 cm resolution)
- Ortho (3 cm resolution)
- HS (10 cm resolution)
- original RGB drone images
- Agisoft Metashape Processing Report

All products are also available as a cloud optimized geotiff.

en: To map and assess snow depth on different dates, 9 flights were conducted in the winter season of 2020/21 at the Latschüelfurgga in Davos. The data was captured with a Sony RX1R II mounted on a Wingtra drone and was processed with the Agisoft Metashape software. High-resolution DSMs, orthomosaics and snow height rasters, as well as the original RGB images from each flight are available.

drone-data

display_name: drone-data

dsm

display_name: dsm

orthophoto

display_name: orthophoto

photogrammetry

display_name: photogrammetry

snow-depth-mapping

display_name: snow-depth-mapping

uav

display_name: uav

wingtra

display_name: wingtra

en: Photogrammetric Drone Data Latschuelfurgga


en: species-richness-models insects species-abundance-distributions spiders urbanization diversity urban-ecology sdms arthropods birds snails

en: contains the raw data to perform species distribution models, only for common species

en: contains the raw data to perform the species richness models of the rare species

en: abundance and occurrence data of the 1446 species studied, used to investigate species-abundance distributions and species-occurrence distributions

en: contains the raw data to perform the species richness models of the hypercommon species

en: contains the raw data to perform the species richness models of all species

en:
Richness, site occurrence and abundance data of bees, beetles, birds, hoverflies, net-wingeds, true bugs, snails, spiders, milipides, wasps collected in the city of Zurich using different sampling techniques, and the environmental variables for each sampling site.
Data are provided on request to contact person against bilateral agreement.

arthropods

display_name: arthropods

birds

display_name: birds

diversity

display_name: diversity

insects

display_name: insects

sdms

display_name: sdms

snails

display_name: snails

species-abundance-distributions

display_name: species-abundance-distributions

species-richness-models

display_name: species-richness-models

spiders

display_name: spiders

urban-ecology

display_name: urban-ecology

urbanization

display_name: urbanization

educ

en: Education, culture and sport

en: Ecological properties of urban ecosystems. Biodiversity dataset of Zurich


data-analysis-toolkits

title_for_slug: data-analysis-toolkits

en: uncertainty statistics error-propagation data-analysis hypothesis-testing bayesian-inference

en: Toolkit 8: Hodges-Lehmann estimators

en: A quick introduction to Hodges-Lehmann estimators (nonparametric measures of effect size)

en: toolkit 6: averaging in nonlinear functions

en: The average of a nonlinear function will not equal the function evaluated at its average inputs (the mean of the function will differ from from the function of the mean). This toolkit shows how to estimate that averaging bias.

en: Toolkit 7: hypothesis testing, significance, and power

en: An overview of basic concepts -- and common pitfalls -- in statistical hypothesis testing, statistical significance, and power analysis

en: Toolkit 1: graphically displaying data distributions

en: Toolkit 11: serial correlation

en: Tools for detecting and correcting for serial correlation in analyses of time series

en: Toolkit 2: quantifying data distributions using descriptive statistics

en: Toolkit 12: weighted averages and their uncertainties

en: There are two different ways to calculate the uncertainty of a weighted average. Software packages often don't tell you which one they are reporting, and the resulting errors can be huge.

en: Toolkit 3: tools for transforming data

en: The ladder of powers and a few other cool transformations

en: Toolkit 5: uncertainty analysis and error propagation

en: Gaussian error propagation, monte carlo methods, and first-order, second-moment error propagation

en: Toolkit 10: linear regression

en: An overview of the math, logic, and pitfalls of ordinary least-squares linear regression

en: Toolkit 9: Experimentwise error rates and statistical fishing expeditions

en: Statistical fishing expeditions, and how to avoid being misled by them

en: Toolkit 4: confidence intervals

en:
These are condensed notes covering selected key points in data analysis and statistics. They were developed by James Kirchner for the course "Analysis of Environmental Data" at Berkeley in the 1990's and 2000's. They are not intended to be comprehensive, and thus are not a substitute for a good textbook or a good education!

License: These notes are released by James Kirchner under a Creative Commons Attribution-ShareAlike 4.0 International (CC BY-SA 4.0) license.

bayesian-inference

display_name: bayesian-inference

data-analysis

display_name: data-analysis

error-propagation

display_name: error-propagation

hypothesis-testing

display_name: hypothesis-testing

statistics

display_name: statistics

uncertainty

display_name: uncertainty

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: Data analysis toolkits


maintainer: Loïc Pellissier Pellissier

en: community-indices herbivores-communities environmental-gradients plant-herbivore-interactions functional-traits alps elevation

en: Orthoptera surveys

en: Species inventories of Orthoptera

en: Orthoptera traits

en: Orthoptera functional traits (incisive mandibular strength averaged by species)

en: Study sites

en: Coordinates and elevation of the study sites

en: Plant traits

en: Plant functional traits (SLA, LDMC, carbon and nitrogen content, punch strenght; averaged by species)

en: Nematode surveys

en: Surveys of soil nematode along elevation

en: Vegetion surveys

en: Species inventories of plants

en: Despite the common role of above- and below-ground herbivore communities in mediating ecosystem functioning, our understanding of the variation of species communities along natural gradient is largely strongly biased toward aboveground organisms. This dataset enables to study the variations in assemblages of two dominant groups of herbivores, namely, aboveground orthoptera and belowground nematodes together with their food plants. Herbivores and plant surveys were conducted in 48 natural grasslands along six elevation gradients, selected to span the major macro-climatic and environmental conditions of the Swiss Alps. It compiles herbivores and plant surveys, information on the study sites as well as plant and herbivores functional traits sought to be involved in trophic interactions and to respond to climatic variation along the elevation. Plant functional traits considered are the SLA, the LDMC, the C/N content, the punch strength (i.e. force required to pierce the leave lamina), the mandibular strength for Orthoptera insect. Data were collected during the summer 2016 and 2017.

alps

display_name: alps

community-indices

display_name: community-indices

elevation

display_name: elevation

environmental-gradients

display_name: environmental-gradients

functional-traits

display_name: functional-traits

herbivores-communities

display_name: herbivores-communities

plant-herbivore-interactions

display_name: plant-herbivore-interactions

educ

en: Education, culture and sport

en: Above- and below-ground herbivore communities along elevation


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

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

complex-terrain

display_name: complex-terrain

cosmo-wrf

display_name: cosmo-wrf

grayzone

display_name: grayzone

numerical-simulation

display_name: numerical-simulation

wrf

display_name: wrf

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


en: cable-yarding seilaplan wms-data geoinformation-system swiss-geodata qgis-plugin digital-elevation-model digital-planning open-source

en: WMS-Layer als Hintergrundkarten laden

en: View video on youtube!

en:
In order to digitally plan a cable line using the QGIS plugin ‘Seilaplan’, maps with various background information are helpful. In this tutorial we show you how to obtain maps that are helpful for cable line planning, for example a national map of Switzerland at different scales, the NFI vegetation height model or the NFI forest mix rate. For this we explain what WMS datasets are and how to integrate them into QGIS. No download of large data is needed for this, only a good internet connection. Please note that the tutorial language is German!

Link for the integration of WMS data: https://wms.geo.admin.ch/

Link to the description on the Swisstopo website:
https://www.geo.admin.ch/en/geo-services/geo-services/portrayal-services-web-mapping/web-map-services-wms.html

Link to the Seilaplan website: https://seilaplan.wsl.ch

**************************

Für die Verwendung des QGIS Plugins Seilaplan zur digitalen Seillinienplanung sind verschiedene Hintergrundkarten hilfreich. In diesem Tutorialvideo zeigen wir, was WMS Daten sind und wie man diese in QGIS einbinden kann. Dafür müssen die Daten nicht heruntergeladen werden. Es braucht lediglich eine gute Internetverbindung. Für die Seillinienplanung hilfreiche Karten sind bspw. die Landeskarte der Schweiz in verschiedenen Massstäben, das Vegetationshöhenmodell LFI oder der Waldmischungsgrad LFI.

Link zur Einbindung der WMS Daten: https://wms.geo.admin.ch/

Link zur Beschreibung auf der Swisstopo Webseite: https://www.geo.admin.ch/de/geo-dienstleistungen/geodienste/darstellungsdienste-webmapping-webgis-anwendungen/web-map-services-wms.html

Link zur Seilaplan-Website: https://seilaplan.wsl.ch

cable-yarding

display_name: cable-yarding

digital-elevation-model

display_name: digital-elevation-model

digital-planning

display_name: digital-planning

geoinformation-system

display_name: geoinformation-system

open-source

display_name: open-source

qgis-plugin

display_name: qgis-plugin

seilaplan

display_name: seilaplan

swiss-geodata

display_name: swiss-geodata

wms-data

display_name: wms-data

en: Seilaplan Tutorial: Load WMS layers as background maps


en: modelling land-use machine-learning land-cover landscape-change landscape

en:
Code used to produce the Land-use/land-cover forecasts for Switzerland across the 21st century at 100-m resolution.
The script is based on input data which are not included as they are not freely available, therefore it will not run as it is. These input data are described in the accompanying publication on Data Science access to them can be requested to their owners. Alternatively the code can be modified to run on other data.

en: Compressed (.zip) file containing six georeferenced raster files in the GeoTIFF format with embedded coordinate reference system, and a table (comma separated values, .csv) encoding a colour palette for plotting (HEX colour codes for each class). GeoTIFF file names include the time-step and the RCP (e.g. “LULC_2020_2049_RCP45.tiff”). Each raster file has 3484x2207 square pixels (i.e. 7.7 megapixels) and is projected in the Swiss coordinate system CH1903+/LV95 (EPSG:2056).

en: We present forecasts of land-use/land-cover (LULC) change for Switzerland for three time-steps in the 21st century under the representative concentration pathways 4.5 and 8.5, and at 100-m spatial and 14-class thematic resolution. We modelled the spatial suitability for each LULC class with a neural network (NN) using >200 predictors and accounting for climate and policy changes. We used data augmentation to increase performance for underrepresented classes, resulting in an overall quantity disagreement of 0.053 and allocation disagreement of 0.15, which indicate good model performance. These class-specific spatial suitability maps outputted by the NN were then merged in a single LULC map per time-step using the CLUE-S algorithm, accounting for LULC demand for the future and a set of LULC transition rules. As the first LULC forecast for Switzerland at a thematic resolution comparable to available LULC maps for the past, this product lends itself to applications in land-use planning, resource management, ecological and hydraulic modelling, habitat restoration and conservation.

land-cover

display_name: land-cover

land-use

display_name: land-use

landscape

display_name: landscape

landscape-change

display_name: landscape-change

machine-learning

display_name: machine-learning

modelling

display_name: modelling

en: High resolution land use forecasts for Switzerland in the 21st century