maintainer: EnviDat Support

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

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:
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 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 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:
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:
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:
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:
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

envidat

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


en: snow snow-temperature uav antarctica irra sea-ice drone snow-roughness

state: active

type: dataset

media_type: application/zip

format: ZIP

en:
This dataset accompanies the publication "How Flat is Flat? Investigating the spatial variability of snow surface temperature and roughness on landfast sea ice using UAVs in McMurdo Sound, Antarctica".
The dataset consists of 1) processed orthomosaic of RGB values, snow topography (digital elevation model), and surface temperature, 2) topography-dependent irradiance map, and 3) point data of measured radiation and atmospheric parameters in the McMurdo Sound, October-December 2022. The data was collected as part of the New Zealand Marsden Fund Research Grant 21-VUW-103 "Can Snow Change the Fate of Antarctic Sea Ice?". Unprocessed data associated with this field campaign are published in 10.16904/envidat.633.
For the airborne measurements, we used a DJI Matrice 30T, a multi-rotor (quadcopter) UAV with self-heating batteries, suitable for operations in polar conditions (temperature range from -20 to +50 °C). The UAV has a wide-angle camera (12 megapixels) for RGB images and a thermal camera (Uncooled Vox Microbolometer, long-wave infrared spectrum 8-14 µm, 1.31 megapixels) for TIR images with an accuracy of ±2 °C or ± 2 %.
GNSS data includes high-precision location information (latitude, longitude, ellipsoidal height, receiver clock offset, and timestamps formatted in decimal hours and day-of-year notation).
WE calculated the distribution of received solar irradiance over the sea-ice surface using a terrain-corrected radiative transfer model and measured shortwave radiation components, accounting for surface roughness, aspect, slope, and solar position during the flight, while applying terrain shading and measured diffuse radiation.
The broadband radiation station data consists of shortwave (Sw) and longwave (Lw) radiation measurements (Kipp & Zonen CMP22 pyranometers and CGR4 pyrgeometers).
Surface temperature readings from cold, sediment, and hot targets were recorded using Apogee SI-121-SS sensors.
This dataset also contains automated weather station (AWS) data (air and snow surface temperatures, relative humidity, wind direction, and wind speed).
For detailed information, please use the README file.

antarctica

display_name: antarctica

drone

display_name: drone

irra

display_name: irra

sea-ice

display_name: sea-ice

snow

display_name: snow

snow-roughness

display_name: snow-roughness

snow-temperature

display_name: snow-temperature

uav

display_name: uav

educ

fr: Éducation, culture et sport

de: Bildung, Kultur und Sport

en: Education, culture and sport

it: Istruzione, cultura e sport

fr: EnviDat: le portail de données environnementales

de: EnviDat: das Umwelt-Datenportal

en: EnviDat: the Environmental Data Portal

it: EnviDat: il portale dei dati ambientali

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

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

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

political_level: other

wsl

capacity: public

type: organization

approval_status: approved

key: guid

key: uri

value: Envidat Harvester

en: Snow On Antarctic Sea Ice - McMurdoSound 2022 - UAV Retrievals of Snow Topography and Snow Surface Temperature


maintainer: Frank Techel

en: avalanche-danger switzerland extended-column-test avalanche-observations norway rutschblock-test

en: ECT data (Norway, Switzerland)

media_type: text/csv

format: CSV

mimetype: text/csv

en: avalanche occurrence data (Norway, Sitzerland) - largest avalanche size per day and warning region

en: avalanche occurrence data (Norway, Sitzerland) - avalanche sizes per day and warning region

en: Rutschblock data (Switzerland)

en:
Observational data used to quantitatively describe the key elements describing avalanche danger: snowpack stability, the frequency distribution of snowpack stability, and avalanche size.
The data set consists of
- Rutschblock test results (Switzerland)
- Extended Column Test results (Switzerland, Norway)
- Avalanche occurrence data (Switzerland, Norway).
The data were extracted from the respective operational databases of the national avalanche warning services in Switzerland (WSL Institute for Snow and Avalanche Research SLF Davos, Switzerland) and Norway (The Norwegian Water Resources and Energy Directorate NVE).
For further information regarding the data, please refer to the publication or contact the author.

avalanche-danger

display_name: avalanche-danger

avalanche-observations

display_name: avalanche-observations

extended-column-test

display_name: extended-column-test

norway

display_name: norway

rutschblock-test

display_name: rutschblock-test

switzerland

display_name: switzerland

en: Stability tests, avalanche observations, Switzerland, Norway


maintainer: Aline Frossard

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

en: Bacterial amplicon sequencing

en: Bacterial ASVs and taxonomic tables

format: XLS

en: Fungal amplicon sequencing

en: Fungal ASVs and taxonomic tables

en: Microbial functions and metadata

en: Extracellular enzyme activities, respiration and sites metadata

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

beta-diversity

display_name: beta-diversity

ecosystem-functions

display_name: ecosystem-functions

microbial-biodiversity

display_name: microbial-biodiversity

microbial-respiration

display_name: microbial-respiration

soil-respiration

display_name: soil-respiration

en: Chicken Creek 10 years


maintainer: Achille Capelli

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

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

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

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

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

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

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

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

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

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

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

en: Manual profiles

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

format: SERVICE

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

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

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

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

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

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

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

en: Webcam images

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

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

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

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

gnss

display_name: gnss

gps

display_name: gps

liquid-water-content

display_name: liquid-water-content

lwc

display_name: lwc

snow-water-equivalent

display_name: snow-water-equivalent

envidat

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

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


en: subalpine first-order-catchment snow runoff alptal meteorological-data

en: Runoff daily mean Alptal 1968-2024 EnviDat updated

en: Runoff, water temperature and electrical conductivity have been measured since 1968 at the outlet of three torrential catchments (with an area of approximately 1 km2 each) located in the Alptal valley: Erlenbach, Lümpenenbach and Vogelbach. This data set provides daily mean values; data at 10-min resolution can be provided on request for the period 1984-2024 (contact: alptal@wsl.ch).

en: Meteorological data Alptal 1968-2024 EnviDat updated

en:
Air temperature, dew point temperature, relative humidity, wind speed, precipitation and global radiation have been measured (since 1981) on a meadow (Erlenhöhe) in the Erlenbach catchment. It is located at 1'220 m a.s.l. with an exposure towards west. In order to assess the spatial variability of precipitation, two additional rain gauges have been running in the Vogelbach and Lümpenenbach catchment, respectively. For the period before 1981, meteorological variables have been extrapolated from the nearby MeteoSwiss station Einsiedeln (ca. 15 km north) to the WSL station Erlenhöhe using a linear correction factor for air temperature, wind speed and precipitation. Snow depth has been recorded automatically since 2003. Snow water equivalent has been calculated using two numerical models: COUP model (Jansson, 2012) and DeltaSnow model (Winkler et al., 2021)
Jansson, P.-E. (2012). COUP model: model use, calibration, and validation.Transactions of the ASABE, 55(4), 1335–1344. Winkler, M., et al. (2021): Snow water equivalents exclusively from snow depths and their temporal changes: the Δsnow model, Hydrol. Earth Syst. Sci., 25, 1165-1187, 10.5194/hess-25-1165-861 2021.

en: Daily meteorological and snow data (1968-2022) Alptal

en:
Air temperature, dew point temperature, relative humidity, wind speed, precipitation and global radiation have been measured (since 1981) on a meadow (Erlenhöhe) in the Erlenbach catchment. It is located at 1'220 m a.s.l. with an exposure towards west. In order to assess the spatial variability of precipiation, two additional rain gauges have been running in the Vogelbach and Lümpenenbach catchment, respectively.
For the period before 1981, meteorological variables have been extrapolated from the nearby MeteoSwiss station Einsiedeln (ca. 15 km north) to the WSL station Erlenhöhe using a linear correction factor for air temperature, wind speed and precipitation.
Snow depth has been recorded automatically since 2003. Snow water equivalent has been calculated using two numerical models: COUP model (Jansson, 2012) and DeltaSnow model (Winkler et al., 2021)

Jansson, P.-E. (2012). COUP model: model use, calibration, and validation.Transactions of the ASABE, 55(4), 1335–1344.
Winkler, M., et al. (2021): Snow water equivalents exclusively from snow depths and their temporal changes: the Δsnow model, Hydrol. Earth Syst. Sci., 25, 1165-1187, 10.5194/hess-25-1165-861 2021.

en: Snow measurements Alptal 1969-2024 EnviDat updated

en: Snow depth, snow density and snow water equivalent have been measured since winter 1968/69 along more than 15 transects distributed across the Alptal valley representing different altitudes, aspects and land use (closed forest and open meadows). Length of the snow courses: 20 to 30 m. The measurement interval has been weekly to monthly. More details about the locations and methods can be found in Stähli, M.; Gustafsson, D., (2006). Long-term investigations of the snow cover in a subalpine semi-forested catchment. Hydrological Processes, 20, 411-428. doi: 10.1002/hyp.6058.

en: Manual snow measurements Alptal (1968-2022)

en: Daily runoff data from three steep torrents in the Alptal (1968-2022)

en: Runoff, water temperature and electrical conductivity have been measured since 1968 at the outlet of three torrential catchments (with an area of approximately 1 km2 each) located in the Alptal valley: Erlenbach, Lümpenenbach and Vogelbach. This data set provides daily mean values; data at 10-min resolution can be provided on request for the period 1984-2022 (contact: alptal@wsl.ch).

en:
This data set includes 56 years of hydrometeorological measurements from small (first-order) catchments in the pre-alpine valley Alptal. Here we provide daily mean values; values in hourly or 10-min resolution can be provided on demand.
Runoff has been measured at the outlet of three small (first-order) catchments of approximately 1 km2 area: Erlenbach (two independent runoff measurements), Vogelbach and Lümpenenbach. The catchments are similar with regard to geology (Flysch) and soil conditions (clay soils), but differ in forest coverage (20 to 60%). A detailed description of the catchments can be found at https://www.wsl.ch/alptal .
Runoff in these small catchments is typically very dynamic and can temporally carry large amounts of sediment and large wood. Thus, the accuracy of the measurements at very large flow is limited.
Meteorological variables have been measured on a meadow (Erlenhöhe) located in the Erlenbach catchment at 1220 m a.s.l. using a standard meteorological station (incl. ventilated air temperature and heated rain gauges). In addition, precipitation has also been recorded at two other locations (in the Vogelbach and Lümpenenbach catchments).
Snow measurements have been conducted weekly to monthly since 1968 at more than 15 locations (30-m transects) representing different altitudes, aspects and land uses (meadow, forest). In addition, snow depth has been recorded continuously since 2003 at Erlenhöhe, and for this location we also include a simulation of snow depth and SWE (using the numerical models COUP and DeltaSnow) that assimilates the manual weekly snow-course measurements. Details on these snow measurements can be found in Stähli, M. and Gustafsson, D. 2006. Hydrol. Proc., 20, 411-428. doi: 10.1002/hyp.6058.
Further information on the methods and sensors can be found at https://www.wsl.ch/alptal .
A first version of this data set (for the period 1968-2017) was uploaded in June 2018 at the occasion of the 50-year anniversary. This original data set was updated in February 2021 (with data from 2018 and 2019), and this data set was used for a longterm trend analysis, submitted for publication in a special issue of Hydrological Processes. Further updates of the data set (with data from 2020 to 2022) were uploaded in March 2023, February 2024 and March 2025.

alptal

display_name: alptal

first-order-catchment

display_name: first-order-catchment

meteorological-data

display_name: meteorological-data

runoff

display_name: runoff

snow

display_name: snow

subalpine

display_name: subalpine

educ

en: Education, culture and sport

en: EnviDat: the Environmental Data Portal

en: Longterm hydrological observatory Alptal (central Switzerland)


en: land-use-change digital-zoning-plans land-use-transformations spatial-planning land-use-simulations

en: Legend simulated maps

en:
Table of Content: 1. General context of the data set "LUSzoning”; 2. Background and aims of the study using the data set LUSzoning; 3. The data set LUSzoning.
1. General context of the data set "LUSzoning".
The data set "LUSzoning" stands for Land-use simulations integrating zoning regulations in Spanish functional urban areas. The data set has been generated as part of the CONCUR research project (https://www.wsl.ch/en/projects/concur.html) led by Dr. Anna M. Hersperger and funded by the Swiss National Science Foundation (ERC TBS Consolidator Grant (ID: BSCGIO 157789) for the period 2016-2021. The CONCUR research project is interdisciplinary and aims to develop a scientific basis for adequately integrating spatial policies (in this case, digital zoning plans) into quantitative land-change modelling approaches at the urban regional level.
2.	Background and aims of the study using the data set “LUSzoning”.
As part of the CONCUR project, a specific task was to integrate planning spatial policies in land-change modelling. Planning can be implemented in modelling using either hard or gradual restrictions. Different studies have addressed the inclusion of spatial planning policies in land-use change modelling. However, the integration of zoning constraints is generally established as hard or Boolean-based restrictions (e.g., whether urban development is allowed or not), while not accounting for the spatial heterogeneity or gradual characteristics within planning zones (e.g., whether planning regulations allow low, medium or high urban density), though these could improve real patterns simulations in urban areas. We assume Spanish General Zoning plans were suitable to explore the integration of planning into land-change modelling as soft constrains because they define land-use intensities in the buildable zoning areas. In light of the above considerations, the overall aim of the study was to model urban land-use changes using a multi-scenario approach that integrates digitized zoning plans for the Functional Urban Areas (FUAs) of Madrid, Barcelona, Valencia, and Zaragoza. The following specific objectives were addressed: i) to analyse the role of planning by defining three future scenarios that integrate digitized zoning plans and one scenario that assumes almost no planning intervention; ii) to introduce zoning constraints that reflect different degrees of urban densities; iii) to generate a transferable spatially-explicit modelling framework to integrate planning into land-use change simulations.
Four future land-use demands scenarios were defined for the FUAs. Storylines were created considering probable development scenarios related to zoning plans, current Spanish legislation and sustainability goals defined along two axes: a high market-oriented vs. high planning-intervention axis, and an axis of short-term economic growth vs. long-term sustainable growth. The sustainable development scenario (S1) is characterized by low gross floor area (GFA) growth that is limited to areas that are currently under development according to zoning plans. The business-as-usual scenario (S2) is characterized by medium GFA growth in the range of on-going trends. The strong development scenario (S3) is characterized by high GFA growth rates. Growth is restricted to buildable areas without urbanization project designated in zoning plans. The unrestricted development scenario (S4) prioritizes a high degree of market liberalization characterized by high GFA growth that surpasses population demands. S4 follows a rapid economic growth pattern with almost no planning intervention.
3.	 The data set “LUSzoning”.
The dataset includes 16 .asc raster layers providing the simulated land-uses under four defined scenarios for Barcelona, Madrid, Valencia and Zaragoza Functional Urban Areas (FUAs) for 2030. The simulated raster layers were created using CLUMondo simulation framework and have a spatial resolution of 30m. The .asc layers name include the name of the FUA and scenario number. For example, the output from simulating the urban growth for the city of Zaragoza under Scenario 2 is named “Zaragoza_S2.tif”. Furthermore, a .txt file named “Legend.txt” includes the numeric value of the land-use and the category of land-use that represents to interpret the .asc raster layers. The name of the land-use classes is a reclassification of the Urban Atlas 2012 land-use classes within the four Spanish FUAs analyzed.

digital-zoning-plans

display_name: digital-zoning-plans

land-use-change

display_name: land-use-change

land-use-simulations

display_name: land-use-simulations

land-use-transformations

display_name: land-use-transformations

spatial-planning

display_name: spatial-planning

envidat

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

en: LUSzoning: Land-use simulations integrating zoning regulations in Spanish functional urban areas


maintainer: Izabela Bujak-Ozga

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

media_type: application/pdf

format: PDF

en: The dataset contains time series of water levels, precipitation measured in the two sub-catchments of the Erlenbach catchment and its vicinity during summer and autumn 2021, 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

data

display_name: data

dataset

display_name: dataset

drainage

display_name: drainage

drainage-network

display_name: drainage-network

dynamics

display_name: dynamics

erlenbach

display_name: erlenbach

precipitation

display_name: precipitation

water-level

display_name: water-level

en: Short-term Drainage Density Dynamics Dataset for the Erlenbach Catchment


en: sentinel-2 time-series tree-species switzerland remote-sensing

en: Tree species profiles for 2020, Red-Edge-2 band

en: Tree species profiles for 2019, Green band

en: Tree species profiles for 2020, CIre index

en: Tree species profiles for 2019, SWIR-2 band

en: Tree species profiles for 2020, SWIR-1 band

en: Tree species profiles for 2020, Red-Edge-1 band

en: Tree species profiles for 2019, NDVI index

en: Tree species profiles for 2020, SWIR-2 band

en: Tree species profiles for 2020, Red band

en: Tree species profiles for 2019, SWIR-1 band

en: Tree species profiles for 2019, CIre Index

en: Tree species profiles for 2020, Green band

en: Tree species profiles for 2020, NDMI index

en: Tree species profiles for 2020, Blue band

en: Tree species profiles for 2020, CCI index

en: Tree species profiles for 2019, NIR band

en: Tree species profiles for 2020, NIR band

en: Tree species profiles for 2019, Blue band

en: Tree species profiles for 2019, CCI index

en: Tree species profiles for 2020, NDVI index

en: Tree species profiles for 2019, Red-Edge-2 band

en: Tree species profiles for 2019, Red band

en: Tree species profiles for 2019, Red-Edge-3 band

en: Tree species profiles for 2019, Red-Edge-1 band

en: Tree species profiles for 2019, NDMI/NDWI index

en: Tree species profiles for 2019, EVI index

en: Tree species profiles for 2020, Red-Edge-3 band

en: Tree species profiles for 2020, EVI index

en:
 Tree species profiles from Sentinel-2 time series
We obtained tree species-specific Sentinel-2 time series for the years 2019 and 2020. The Sentinel-2 time series originated from [here](https://www.envidat.ch/#/metadata/sentinel-2-time-series-of-switzerland), and the tree species information was derived from pure plots of the Swiss National Forest Inventory, spread all over Switzerland.
In addition to the 10 and 20 m bands from Sentinel-2 (Blue, Green, Red, Red-Edge-1, Red-Edge-2, Red-Edge-3, NIR, SWIR-1, SWIR-2), we calculated indices (CCI, CIre, EVI, NDMI/NDWI, NDVI).
In total, tree species profiles of 763 pixels for 2020 and 562 pixels for 2019 are available for seven tree species (*Abies alba*, *Castanea sativa*, *Fagus sylvatica*, *Fraxinus excelsior*, *Larix* spp., *Picea abies*, *Pinus sylvestris*).

remote-sensing

display_name: remote-sensing

switzerland

display_name: switzerland

time-series

display_name: time-series

tree-species

display_name: tree-species


en: glide-snow-avalanche soil-moisture avalanche-activity avalanche snow-profile

en: This file contains SNOWPACK simulations (snow height, air temperature, rain) at a virtual station in the reference location. The virtual station was interpolated between the Weissfluhjoch (WFJ2) and Klosters Madrisa (KLO2) IMIS Stations.

en: This file contains all sensor recordings in the Seewer Berg slope (time interval: 15 minutes).

en: This file contains the coordinates of the reference location and the sensors in the Seewer Berg slope as a shapefile.

en: This file contains all soil measruements (liquid water content and matric potential) recorded at the reference location.

media_type: text/plain

en: This file explains all provided datasets, variables and their units.

format: TXT

en: This file provides an overview of the dataset, the detailed measurement setup, and points out limitations.

en: This file contains the release areas (polygon) of glide-snow avalanches as a shapefile.

en: This file contains the aggregated data from manually recorded snow profiles in the reference location, 100m northwest of the Seewer Berg slope and in release areas of glide-snow avalanches in the Seewer Berg slope.

en: This file contains the daily avalanche activity on Dorfberg as extracted from time-lapse photographs.

en:
This dataset consists of spatio-temporal soil measurements and local snow measurements which were recorded to investigate glide-snow avalanche release in the Seewer Berg slope (Davos, Switzerland) from Nov 2021 to June 2024. Investigations based on this dataset were published in the research article:
Fees A., Lombardo M., van Herwijnen A., Lehmann P., Schweizer J. (2025). The source, quantity, and spatial distribution of interfacial water during glide-snow avalanche release: experimental evidence from field monitoring. The Cryosphere
The dataset consists of:
- Soil measurements (temperature and liquid water content) at soil depths of -5cm, -10cm, and -20cm
- Matric potential at depths of -5cm, -10cm, and -20cm
- Manual snow profiles (Snow height, temperature, liquid water content, bulk density)
- Metadata and manual snow profiles on glide-snow avalanches that released in the Seewer Berg slope
- Snow height, air temperature and rain simulated with SNOWPACK.

avalanche

display_name: avalanche

avalanche-activity

display_name: avalanche-activity

glide-snow-avalanche

display_name: glide-snow-avalanche

snow-profile

display_name: snow-profile

soil-moisture

display_name: soil-moisture

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: Spatio-temporal soil and local snow monitoring in a glide-snow avalanche prone slope above Davos Switzerland


maintainer: Lyu

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

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

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

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

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

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

fagales

display_name: fagales

pinales

display_name: pinales

species-distribution-model

display_name: species-distribution-model

species-occurrence

display_name: species-occurrence

species-range-map

display_name: species-range-map

species-richness

display_name: species-richness

en: Species distribution maps of Fagales and Pinales (GDPlants)


en: clouds raclets backward-trajectories aerosol ice-nucleation

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

aerosol

display_name: aerosol

backward-trajectories

display_name: backward-trajectories

clouds

display_name: clouds

ice-nucleation

display_name: ice-nucleation

raclets

display_name: raclets

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


maintainer: Tobias Wechsler

en: schweiz kleinstwasserkraftwerke speed2zero wasserkraft datensatz

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

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

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

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

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

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

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

datensatz

display_name: datensatz

kleinstwasserkraftwerke

display_name: kleinstwasserkraftwerke

schweiz

display_name: schweiz

wasserkraft

display_name: wasserkraft

en: CH-Kleinstwasserkraftwerke - ein schweizweiter Datensatz zu Kleinstwasserkraftwerken


en: life-history-traits performance-traits cavity-nesting cities urban-ecology wasps hymennoptera hymenoptera natural-enemies bees richness urbanization

en: Taxonomic metrics on CNBW

en:
The data contains at the site level the species richness of cavity-nesting bees and wasps. It also contains site level estimates of the life-history traits and the performance traits.

We calculated species richness, abundance, and number of nests of the hatched hosts separately for bees and wasps. We calculated the abundance of hatched hosts as the number of brood cells where an individual emerged, i.e. the total number of brood cells minus the number of parasitized cells and the number of cells with no emergence for reasons other than parasitism.

City codes: An =Antwerp, Pa = Paris; Po = Poznan; Ta =Tartu; Zu= Zurich

en: Information on the study sites

en: For each site, the IDs, city, coordinates, structure where the trapnest was attached and height is provided

en: Taxonomic metrics on the natural enemies

en: It contains the species richness and the abundance of natural enemies per site.

en: Performance traits and life-history traits

en:
It contains the data of two performance traits (survival and parasitism) and two life-history traits (sex ratio and number of offspring per nest for the hosts) at the nest level.

We assessed performance traits, i.e. survival and parasitism, at the individual cell level. Specifically, for each cell within a nest, we noted whether the cell was alive or dead (survival), and whether it had a parasite or not (parasitism). Further, we calculated the parasitism rate as the number of cells with a parasite divided by the total number of cells. Concerning life-history traits, we calculated the total number of brood cells per nest as the total number of brood cells within a single nest, regardless of whether the larvae were dead, alive or parasitized. Finally, we used the probability that a femalehost emerged from a given cell as a proxy for the sex ratio. To do so, we first identified the sex of the individual hosts. Then, we noted it in a binary way to indicate whether the host was a female or not. We could identify the sex of all hatched hosts. Further, because CNBW first lay females and then males, on some occasions we could also identify the host sex in dead and parasitized cells, that is, when we had already identified the sex of the preceding and the following cells.

en: Predictors of the study

en:
 Background
Urban ecosystems are associated with socio-ecological conditions that can filter and promote taxa. However, the strength of the effect of ecological filtering on biodiversity could vary among biotic and abiotic factors. Here, we provide the data used to investigate the effects of habitat amount, temperature, and host-enemy biotic interactions in shaping communities of cavity-nesting bees and wasps (CNBW) and their natural enemies. To do so, we installed trap-nests in 80 sites distributed along urban intensity gradients in 5 European cities (Antwerp, Paris, Poznan, Tartu and Zurich). We quantified the species richness and abundance of CNBW hosts and their natural enemies, as well as two performance traits (survival and parasitism) and two life-history traits (sex ratio and number of offspring per nest for the hosts).
The dataset contains:
* The taxonomic metrics on CNBW
* The taxonomic metrics on the natural enemies from CNBW
* The life-history traits and performance traits

bees

display_name: bees

cavity-nesting

display_name: cavity-nesting

cities

display_name: cities

hymennoptera

display_name: hymennoptera

hymenoptera

display_name: hymenoptera

life-history-traits

display_name: life-history-traits

natural-enemies

display_name: natural-enemies

performance-traits

display_name: performance-traits

richness

display_name: richness

urban-ecology

display_name: urban-ecology

urbanization

display_name: urbanization

wasps

display_name: wasps

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: Community structure, life-history traits and performance traits of urban cavity-nesting bees annd wasps


maintainer: Matthias Haeni

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

en: Forest station data (VSB)

en: Data file.

en: Field station data (VSF)

en: Site photo of the forest station (VSB)

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

mimetype: image/jpeg

en: Site photo of the field station (VSF)

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

en: Data plot of the field station (VSF)

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

mimetype: application/pdf

en: Site aerial photo (Visp)

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

en: Data plot of the forest station (VSB)

en: High quality meteorological data are needed for long-term forest ecosystem research, particularly in the light of global change. The long-term data series published here comprises almost 20 years of measurements for two meteorological stations in Visp in Switzerland where one station is located within a natural mixed forest stand (VSB) with Scots pine (_Pinus sylvestris_; 40-80 yrs) as dominant tree species. A second station is situated in the very vicinity outside of the forest (field station, VSF). The meteorological time series are presented in hourly time resolution of air temperature, relative humidity, precipitation, photosynthetically active radiation (PAR) and wind speed. Visp is part of the Long-term Forest Ecosystem Research Programme (LWF) established and maintained by the Swiss Federal Research Institute WSL.

climate-change

display_name: climate-change

long-term

display_name: long-term

meteo

display_name: meteo

meteorology

display_name: meteorology

par

display_name: par

precipitation

display_name: precipitation

relative-humidity

display_name: relative-humidity

swiss-forest-lab

display_name: swiss-forest-lab

temperature

display_name: temperature

wind-speed

display_name: wind-speed

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


maintainer: Jokin Idoate-Lacasia

en: carbon-storage forest-inventory biomass-dynamics forest-reserves environmental-gradients

format: OCTET

en: Climatic space covered by the Swiss National Forest Inventory (NFI) that will be used in Figure 5.

en: R markdown document used to download the data files, reproduce the analysis and plot generation.

en:
This dataset documents the analyses and the plot generation for the manuscript **Long-term biomass dynamics in temperate forests in Europe after cessation of management**.
We analyse biomass development in an extensive network of 224 plots in 37 natural forest reserves (NFR) covering a wide environmental gradient with mean annual temperatures ranging from 1 to 10.4 °C and mean annual precipitation ranging from 901 to 2317 mm. Forest inventories have been conducted approximately every 10 years during the last 60 years.
It consists of the following files:
+ **Long_term_biomass_script.Rmd**: R markdown document to reproduce the analysis and the plot generation.
+ **dat_biomass.RDS**: Biomass values for each permanent plot at each inventory. This dataset is used for data exploration and for the Biomass model, and to create Figure 2 and Figure 3.
+ **dat_biomass_change.RDS**: Biomass change values between inventories for each permanent plot. It includes the explanatory variables as well. This dataset is used for the Biomass change model and to create Figure 4 and Figure 5.
+ **NFI_climspace_netCDF.RDS**: Climatic space covered by the Swiss National Forest Inventory (NFI) that is used in Figure 5.

biomass-dynamics

display_name: biomass-dynamics

carbon-storage

display_name: carbon-storage

environmental-gradients

display_name: environmental-gradients

forest-inventory

display_name: forest-inventory

forest-reserves

display_name: forest-reserves

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: Long-term biomass dynamics of temperate forests in Europe after cessation of management


maintainer: Lorenz Walthert

en: anisohydric stomatal-stringency water-potential root-distribution water-use-strategy

en: The data file contains the data shown in the Figures 2-7 in Walthert et al. (2024).

en:
This dataset represents the data shown in the Figures 2 - 7 of Walthert et al. (2024): Coordination between degree of isohydricity and depth of root water uptake in temperate tree species. Science of the Total Environment (https://doi.org/10.1016/j.scitotenv.2024.174346). A detailed methodical description of the data can be found in the Methods section of the paper.

Abstract
In an increasingly dry environment, it is crucial to understand how tree species use soil water and cope with drought. However, there is still a knowledge gap regarding the relationships between species-specific stomatal behaviour, spatial root distribution, and root water uptake (RWU) dynamics.
Our study aimed to investigate above- and below-ground aspects of water use during soil drying periods in four temperate tree species that differ in stomatal behaviour: two isohydric tracheid-bearing conifers, Scots pine and Norway spruce, and two more anisohydric deciduous species, the diffuse-porous European beech, and the ring-porous Downy oak. From 2015 to 2020, soil-tree-atmosphere-continuum parameters were measured for each species in monospecific forests where trees had no access to groundwater. The hourly time series included data on air temperature, vapour pressure deficit, soil water potential, soil hydraulic conductivity, and RWU to a depth of 2 m. Analysis of drought responses included data on stem radius, leaf water potential, estimated osmotically active compounds, and drought damage.
Our study reveals an inherent coordination between stomatal regulation, fine root distribution and water uptake. Compared to conifers, the more anisohydric water use of oak and beech was associated with less strict stomatal closure, greater investment in deep roots, four times higher maximum RWU, a shift of RWU to deeper soil layers as the topsoil dried, and a more pronounced soil drying below 1 m depth. Soil hydraulic conductivity started to limit RWU when values fell below 10-3 to 10-5 cm/d, depending on the soil. As drought progressed, oak and beech may also have benefited from their leaf osmoregulatory capacity, but at the cost of xylem embolism with around 50% loss of hydraulic conductivity when soil water potential dropped below -1.25 MPa. Consideration of species-specific water use is crucial for forest management and vegetation modelling to improve forest resilience to drought.

anisohydric

display_name: anisohydric

root-distribution

display_name: root-distribution

stomatal-stringency

display_name: stomatal-stringency

water-potential

display_name: water-potential

water-use-strategy

display_name: water-use-strategy

en: Water-use strategies of temperate tree species


envidat-supports-open-science

maintainer: Ionut Iosifescu Enescu

title_for_slug: envidat-supports-open-science

en: open-science envidat wsl juypter-notebooks research-data-management

en: Article as PDF

en:
The article "EnviDat Supports Open Science" originally appeared in WSLintern No. 3 (2020), page 14-15 and it is republished here with permission from the WSLintern editorial team. It contains guidelines for WSL scientists about the main issues behind Open Science and how to pragmatically approach the complexities of doing Open Science with EnviDat’s support.

License: This article is released by WSL and the EnviDat team to the public domain under a Creative Commons 4.0 CC0 "No Rights Reserved" international license. You can reuse the information contained herein in any way you want, for any purposes and without restrictions.

envidat

display_name: envidat

juypter-notebooks

display_name: juypter-notebooks

open-science

display_name: open-science

research-data-management

display_name: research-data-management

wsl

display_name: wsl

en: EnviDat Supports Open Science


photogrammetric-drone-data-dorfberg

maintainer: Yves Bühler

title_for_slug: photogrammetric-drone-data-dorfberg

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

en: Data Access

en:
- 3cm-resolution Orthophoto
- 10cm-resolution DSM
- 10cm-resolution snow depth raster
- original RGB images
- Agisoft Metashape Report

All products are also available as a cloud optimized geotiff.

en: The data was collected with a Wingtra Gen II drone and a Sony RX1R II sensor. In total, 10 flights were conducted at different dates, both in summer and winter. A DSM, an orthophoto, a snow depth raster and the original drone images from every flight are available at a high resolution (10cm and 3cm, respectively).

drone-data

display_name: drone-data

dsm

display_name: dsm

orthophoto

display_name: orthophoto

photogrammetry

display_name: photogrammetry

snow

display_name: snow

snow-depth-mapping

display_name: snow-depth-mapping

snow-distribution

display_name: snow-distribution

uav

display_name: uav

en: Photogrammetric Drone Data Dorfberg


maintainer: Yohann Chauvier

en: cluster target-group point-process-model environmental-stratification survey-effort covariate-correction background-data plant-species independent-dataset random-stratified-sampling

en: Non-copyright data, scripts, diversity outputs

en:
Aim: While species distribution models (SDMs) are standard tools to predict species distributions, they can suffer from observation and sampling biases, particularly presence-only SDMs that often rely on species observations from non-standardized sampling efforts. To address this issue, sampling background points with a target-group strategy is commonly used, although more robust strategies and refinements could be implemented. Here, we exploited a dataset of plant species from the European Alps to propose and demonstrate efficient ways to correct for observer and sampling bias in presence-only models.

Innovation: Recent methods correct for observer bias by using covariates related to accessibility in model calibrations (classic bias covariate correction, Classic-BCC). However, depending on how species are sampled, accessibility covariates may not sufficiently capture observer bias. Here, we introduced BCCs more directly related to sampling effort, as well as a novel corrective method based on stratified resampling of the observational dataset before model calibration (environmental bias correction, EBC). We compared, individually and jointly, the effect of EBC and different BCC strategies, when modelling the distributions of 1’900 plant species. We evaluated model performance with spatial block split-sampling and independent test data, and assessed the accuracy of plant diversity predictions across the European Alps.

Main conclusions: Implementing EBC with BCC showed best results for every evaluation method. Particularly, adding the observation density of a target group as bias covariate (Target-BCC) displayed most realistic modelled species distributions, with a clear positive correlation (r≃0.5) found between predicted and expert-based species richness. Although EBC must be carefully implemented in a species-specific manner, such limitations may be addressed via automated diagnostics included in a provided R function. Implementing EBC and bias covariate correction together may allow future studies to address efficiently observer bias in presence-only models, and overcome the standard need of an independent test dataset for model evaluation.

background-data

display_name: background-data

cluster

display_name: cluster

covariate-correction

display_name: covariate-correction

environmental-stratification

display_name: environmental-stratification

independent-dataset

display_name: independent-dataset

plant-species

display_name: plant-species

point-process-model

display_name: point-process-model

random-stratified-sampling

display_name: random-stratified-sampling

survey-effort

display_name: survey-effort

target-group

display_name: target-group

educ

en: Education, culture and sport

en: Novel methods to correct for observer and sampling bias in presence-only species distribution models


en: biogeochemical-cycling wolf bacteria soil-biodiversity carrion fungi carcass detritus decomposition yellowstone

en:
Site	ID for different carcasses across the Yellowstone Landscape
Location	Sampling location, either under carcass or control plot
Species	Indicating whether carcass was from bison or elk
Gender	Gener of carcass; F = female, M = male, ? = unknown
Lat	Latitude
Long	Longitude
DSK	Days since kill; in days
Soil.N	Soil N concentration (%)
Soil.C	Soil C concentration (%)
Veg.C	Vegetation C concentration (%); dominant grasses sampled
Veg.N	Vegetation N concentration (%); dominant grasses sampled
Veg.CtoN	Vegetation C to N ratio; dominant grasses sampled
Soil.resp	Soil respiration (g m-2 h-1)
soil.temp	Soil temperature (°C)
Soil.moist	Soil moisture (volumentric; %)
CRR	Cotton rotting rate
bacteria.richness	Bacteria richness
bacteria.diversity	Bacteria diverstiy
fungi.richness	Fungi richness
fungi.diversity	Fungi diversity
bacteria.abundance	Bacteria abundance
fungi.abundance	Fungi abundance

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

Paper Citation:

Risch, A.C., Frossard, A., Schütz, M., Frey, B., Morris, A.W., Bump, J.K. (accepted) Effects of elk and bison carcasses on soil microbial communities and ecosystem functions in Yellowstone, USA. (accepted). Functional Ecology
doi: ...

Methods
Study area and study sites
This study was conducted in YNP’s Northern Range (NR), located in north-western Wyoming and south-western Montana, USA (~44.9163° N, 110.4169° W). The NR expands over ~1000 km2 and features long cold winters and short dry summers. Grasslands and shrublands dominate the NR that is the home of large migratory herds of bison (winter counts 2017: ~3919 individuals; Geremia, Wallen, & White, 2017) and elk (~5349 individuals) as well as their main predators, approximately five packs of wolves with a total of 33 individuals (Smith et al., 2017). As part of a long-term research program within YNP, wolf predation has been studied since their reintroduction in 1995.
For our study, we received ground-truthed coordinates of bison and elk carcasses from winter 2016/17 (November 2016 through April 2017) from the YNP Wolf Project. Between June 20 and July 1, 2017, we visited 24 carcasses in total. At five sites, we could not sample as the carcasses were no longer found. In total we located remains (hairmats, rumen content, bones, teeth) of 19 adult male and female carcasses (7 bison, 12 elk; Supplementary Table 1). Live body weights of adult bison and elk are approximately 730 kg (male bison), 450 kg (female bison), 330 kg (male elk), and 235 kg (female elk, Meagher, 1973; Quimby & Johnson, 1951).
The kills and subsequent consumption happened between 34 and 173 days prior to our sampling (hereafter “days since kill”, DSK), for which we accounted in our statistics. Note that wolves and other scavengers consumed the soft tissue of the carcasses quickly, hence, there is close to no soft tissue left for decomposition as compared to an intact body left on the soil surface. The 19 carcass sites covered the extent of YNP’s NR, with both bison and elk carcasses showing similar distributions; elevation ranged from 1703 to 2884 m a.s.l. (Supplementary Fig 1 & Supplementary Table 1). The carcasses were all located in grassland or sage-brush shrubland, with or without sparsely scattered trees, and both bison and elk carcasses showed the same distribution of DSK. At each study site, we selected a reference plot (hereafter “control”) that was of comparable size, slope aspect and vegetation to the carcass location (hereafter “carcass”). The control was at least 10 m away (Danell, Berteaux, & Brathen, 2002; Melis et al., 2007) from the carcass itself to ensure the absence of potential direct and indirect carcass effects (paired design; (Bump, Webster, et al., 2009; Bump, Peterson, et al., 2009).

Ecosystem functions and soil properties
We randomly collected 50 g of mineral soil from three locations on both control and carcass plots to a depth of 5 cm with sterile techniques and gently mixed the material to obtain a composite sample. Half the soil sample was immediately bagged in plastic bags (whirl packs), stored in a cooler with ice packs (~5 ºC), sieved (2-mm) and frozen within 4-6 hours of collection to assess soil microbial communities. For this purpose, we extracted total genomic DNA from 0.5 g soil using the PowerSoil DNA Isolation Kit (Qiagen, Hilden, Germany). DNA concentrations were measured using PicoGreen (Molecular Probes, Eugene, OR, USA). PCR amplifications of partial bacterial small-subunit ribosomal RNA genes (region V3–V4 of 16S rRNA) and fungal ribosomal internal transcribed spacers (region ITS2) were performed as described previously (Frey et al., 2016). Each sample consisting of 40 ng DNA was amplified in triplicate and pooled before purification with Agencourt AMPure XP beads (Beckman Colter, Berea, CA, USA) and quantified with the Qubit 2.0 fluorometric system (Life Technologies, Paisley, UK). Amplicons were sent to the Genome Quebec Innovation Center (Montreal, Canada) for barcoding using the Fluidigm Access Array technology and paired-end sequencing on the Illumina MiSeq v3 platform (Illumina Inc., San Diego, CA, USA).
Quality control of bacterial and fungal reads was performed using a customized pipeline (Supplementary Table 2; Frey et al., 2016). Paired-ends reads were matched with USEARCH (Edgar & Flyvbjerg, 2015), substitution errors were corrected using Bayeshammer (Nikolenko, Korobeynikov, & Alekseyev, 2013) and PCR primers were trimmed (allowing for 1 mismatch, read length >300 bp for 16S and >200 bp for ITS primers) using Cutadapt (M. Martin, 2011). Sequences were dereplicated and singleton reads removed prior to clustering into operational taxonomic units (OTUs) at 97% identity using USEARCH (Edgar, 2013). The remaining centroid sequences were tested for the presence of ribosomal signatures using Metaxa2 (Bengtsson-Palme et al., 2015) or ITSx (Bengtsson-Palme et al., 2013). Taxonomic assignments of the OTUs were obtained using Bayesian classifier (Wang, Garrity, Tiedje, & Cole, 2007) with a minimum bootstrap support of 60% implemented in mothur (Schloss et al., 2009) by querying the bacterial and fungal reads against the SILVA Release 128 (Quast et al., 2013) and UNITE 8.0 (Abarenkov et al., 2010) reference databases for 16S and ITS OTUs, respectively.
Abundances of the bacterial 16S rRNA gene and fungal ITS amplicon were determined by quantitative real-time PCR (qPCR) on an ABI7500 Fast Real-Time PCR system (Applied Biosystems, Foster City, CA, USA) as described previously (Frossard et al., 2018). The same primers (without barcodes) and cycling conditions as for the sequencing approach were used for the 16S and ITS qPCR. Three standard curves per target region were obtained using tenfold serial dilutions of plasmids generated from cloned targets (Frey, Niklaus, Kremer, Lüscher, & Zimmermann, 2011). Data were converted to represent mean copy number of targets per gram of soil (dry weight).
The other half of the soil sample was bagged in paper, dried to constant weight at 60°C, passed through a 2 mm sieve and analyzed for total C and N concentration with a CE Instruments NC 2100 soil analyzer (CE Elantech Inc., Lakewood NJ, USA). We also collected 20 mature and undamaged leaves of the dominant grass species growing on control and carcass sites, but taxa were not recorded. The plant material was dried at 60°C, finely ground till homogenized and also analyzed to obtain total C and N concentrations. Soil temperature (10 cm depth) was measured with a waterproof digital thermometer (Barnstead International, Dubuque IA, USA) at three locations each at the control and carcass site. Soil moisture (0 – 10 cm depth) was measured with time domain reflectometry (Field-Scout TDR-100; Spectrum Technologies, Plainfield IL, USA) at five randomly chosen points on control and carcass sites. We measured soil respiration at five randomly chosen points at both control and carcass sites with a PP-Systems SRC-1 soil respiration chamber (closed circuit) attached to a PP-Systems EGM-4 infrared gas analyzer (PP-Systems, Amesbury, MA, USA). For each measurement the soil chamber (15 cm high; 10 cm diameter) was tightly placed on the soil surface, after clipping plants to avoid measuring plant respiration or photosynthesis. Measurements were conducted over 120 s.
In addition, we assessed the decomposition rates of standardized OM using the cotton strip assay (Latter & Howson, 1977; Latter & Walton, 1988). Cotton cloth tensile strength loss (CTSL) is a measure of decomposition, and an index to express the combined effect of soil microclimatic, physical, chemical and biological properties on decomposition while accounting for OM quality (Latter & Walton, 1988; Risch, Jurgensen, & Frank, 2007; Withington & Sanford Jr., 2007). We placed five 20 cm wide x 13 cm long sheets of 100% unbleached cotton cloth (American Type SM 1/18’’, Warp: 34/1, Weft: 20/1, Weave plain, 29.5 picks/cm warp, 22 picks/cm weft, 237 g/m2; Daniel Jenny & Co., Switzerland;) at each carcass and control site vertically into the soil by making slits with a flat spade to a depth of 12 cm. We inserted each cloth with the spade, and then pushed the slit closed to assure tight contact with the soil. The cloths were retrieved after 18 to 27 days. After retrieval, the cloths were air-dried, remaining soil gently removed by hand, and 1.5 cm wide strips were cut at the 3.5-5.0 cm (top) and the 9-10.5 cm (bottom) soil depth. The strips were equilibrated at 50 % relative humidity and 20°C for 48 hours (climate chamber) prior to strength testing (Scanpro Awetron TH-1 tensile strength tester; AB Lorentzen and Wettre, Kista, Sweden). Cotton rotting rate (CRR) = (CTScontrol - CTSfinal/CTSfinal)1/3 * (365/t), where CTScontrol is the cotton tensile strength of a control cloth and CTSfinal the cotton tensile strength of the incubated sample, t is the incubation period in days. Control cloths were inserted into the ground and immediately retrieved to account for tensile strength loss associated with cloth insertion. We averaged the CRR of top and bottom strips for further analyses as no difference was found between the two. All sampling and cloth insertion took place between June 20 and July 1, 2017, cloths were retrieved between July 17 and 20, 2017. Soil respiration, average CRR, vegetation N concentration and vegetation C:N ratio are defined as ecosystem functions, soil C and N concentration, soil temperature and moisture as soil abiotic properties, and bacterial and fungal richness (number of taxa), diversity (Shannon) and abundance as soil biotic properties.

Statistical analyses
Univariate analyses for ecosystem functions, soil biotic and abiotic properties
We tested whether individual ecosystem functions, soil biotic and abiotic properties differed between carcass and control (“Location”), bison and elk (“Species”) and days since kill (“DSK”). For this purpose, we used linear mixed effect models (LMM, “nlme” package v 3.1 – 131.1 in R v 3.4.4; Pinheiro, Bates, DebRoy, & Sarkar, 2018; R Core Team, 2019) with Location, Species, Location x Species and DSK as fixed effects. Site was included as random effect to account for the paired design. We developed a separate model for all dependent variables. All but bacterial richness, fungal richness, fungal diversity and vegetation N concentration were natural-log transformed to meet model assumptions. For each LMM, we calculated contrasts to assess the specific comparisons we were interested in with the “lsmeans” package v 2.27-62 (Lenth & Love, 2018): 1) carcass vs control, 2) carcass bison vs control bison, and 3) carcass elk vs control elk. We also tested whether we had differences between bison and elk carcasses or the sites where bison and elk were killed and included contrasts 4) carcass bison vs carcass elk and 5) control bison vs control elk.
We calculated the log response ratio (LRR = ln[carcass/control]) to obtain carcass effects for all variables for both species separately. LRR < 0 indicates higher value at control compared to carcass, LRR > 0 indicates higher values at carcass compared control. We used LRRs for visualization and to assess spatial patterns in carcass effects across YNP. For this purpose we calculated the Moran’s I statistic for each ecosystem function, soil biotic and abiotic property based on a latitude-longitude matrix with the “moran.test” function in the “spdep” package version 1.1-3 (Bivand et al., 2019).
Multivariate analyses
Rare OTUs, defined as OTUs with a low abundance of reads, were retained in multivariate methods because they only marginally influence these analyses (Gobet, Quince, & Ramette, 2010). Bray–Curtis dissimilarity matrices were generated based on square-root-transformed matrices. We used Principal Coordinate Analyses (PCoA) to assess how soil bacterial and fungal communities differed between control and carcass of bison and elk (“vegan” package v 2.5-4, Oksanen et al., 2019). We then extracted PCoA axes scores 1 and 2 and used LMM (“nlme” package) with Location, Species, Location x Species and DSK as fixed effects. Site was, again, included as random effect. We again calculated the contrasts as described above using the “lsmeans” package. We also assessed how ecosystem functions, and soil abiotic and biotic properties were related to the soil bacteria and fungi community structure associated with bison and elk control and carcasses using the “envfit” function in the “vegan” package (Oksanen et al., 2019).
Indicator species analyses were performed using the multipatt function implemented in the “indicspecies” package version 1.7.6 with 100000 permutations (De Caceres & Jansen, 2016). This step allowed to identify OTUs that led to changes in multivariate patterns between control and carcass of both bison and elk separately (De Cáceres, Legendre, & Moretti, 2010). The multipatt function uses a point biserial correlation coefficient statistical test. Indicator OTUs were defined as bacterial and fungal OTUs with more than 50 sequences, i.e., removing rare taxa and taxa with low abundances containing little indicator information (Rime et al., 2015) and that were significantly correlated with Location (p < 0.05, correlation coefficient > 0.3). A heatmap of these OTUs were generated with the vegan and ggplot2 packages. The indicator analyses were performed in R version 3.3.3 (R Core Team, 2017).

References
Abarenkov, K., Henrik Nilsson, R., Larsson, K.-H., Alexander, I. J., Eberhardt, U., Erland, S., … Kõljalg, U. (2010). The UNITE database for molecular identification of fungi – recent updates and future perspectives. New Phytologist, 186(2), 281–285. doi:10.1111/j.1469-8137.2009.03160.x
Bengtsson-Palme, J., Hartmann, M., Eriksson, K. M., Pal, C., Thorell, K., Larsson, D. G. J., & Nilsson, R. H. (2015). metaxa2: improved identification and taxonomic classification of small and large subunit rRNA in metagenomic data. Molecular Ecology Resources, 15(6), 1403–1414. doi:10.1111/1755-0998.12399
Bengtsson-Palme, J., Ryberg, M., Hartmann, M., Branco, S., Wang, Z., Godhe, A., … Nilsson, R. H. (2013). Improved software detection and extraction of ITS1 and ITS2 from ribosomal ITS sequences of fungi and other eukaryotes for analysis of environmental sequencing data. Methods in Ecology and Evolution, 4(10), 914–919. doi:10.1111/2041-210X.12073
Bivand, R., Altman, M., Anselin, L., Assuncao, R., Berke, O., Blanchet, G., … Yu, D. (2019). spdep: Spatial dependence, weighthing schemes, statistics. R package version 1.1-3.
Bump, J. K., Peterson, R. O., & Vucetich, J. A. (2009). Wolves modulate soil nutrient heterogeneity and foliar nitrogen by configuring the distribution of ungulate carcasses. Ecology, 90(11), 3159–3167.
Bump, J. K., Webster, C. R., Vucetich, J. A., Peterson, R. O., Shields, J. M., & Powers, M. D. (2009). Ungulate carcasses perforate ecological filters and create biogeochemical hotspots in forest herbaceous layers allowing trees a competitive advantage. Ecosystems, 12(6), 996–1007. doi:10.1007/s10021-009-9274-0
Danell, K., Berteaux, D., & Brathen, K. A. (2002). Effect of muskox carcasses on nitrogen concentration in tundra vegetation. Arctic, 55(4), 389392.
De Caceres, M., & Jansen, F. (2016). indicspecies: relationship between species and groups of species. R package version 1.7.6.
De Cáceres, M., Legendre, P., & Moretti, M. (2010). Improving indicator species analysis by combining groups of sites. Oikos, 119(10), 1674–1684. doi:10.1111/j.1600-0706.2010.18334.x
Edgar, R. C. (2013). UPARSE: highly accurate OTU sequences from microbial amplicon reads. Nature Methods, 10, 996.
Edgar, R. C., & Flyvbjerg, H. (2015). Error filtering, pair assembly and error correction for next-generation sequencing reads. Bioinformatics, 31(21), 3476–3482. doi:10.1093/bioinformatics/btv401
Frey, B., Niklaus, P. A., Kremer, J., Lüscher, P., & Zimmermann, S. (2011). Heavy-machinery traffic impacts methane emissions as well as methanogen abundance and community structure in oxic forest soils. Applied and Environmental Microbiology, 77(17), 6060–6068. doi:10.1128/AEM.05206-11
Frey, B., Rime, T., Phillips, M., Stierli, B., Hajdas, I., Widmer, F., & Hartmann, M. (2016). Microbial diversity in European alpine permafrost and active layers. FEMS Microbial Ecology, 92(3), fiw018.
Frossard, A., Donhauser, J., Mestrot, A., Gygax, S., Bååth, E., & Frey, B. (2018). Long- and short-term effects of mercury pollution on the soil microbiome. Soil Biology and Biochemistry, 120, 191–199. doi:https://doi.org/10.1016/j.soilbio.2018.01.028
Geremia, C., Wallen, R., & White, P. J. (2017). Status report of the Yellowstone bison population, September 2017. Yellowstone National Park, Mammoth, WY, USA: National Park Service, Yellowstone Center for Resources.
Gobet, A., Quince, C., & Ramette, A. (2010). Multivariate cutoff level analysis (MultiCoLA) of large community data sets. Nucleic Acids Research, 38(15), e155–e155. doi:10.1093/nar/gkq545
Latter, P., & Howson, G. (1977). The use of cotton strips to indicate cellulose decomposition in the field. Pedobiologia, (17), 145–155.
Latter, P., & Walton, D. (1988). The cotton strip assay for cellulose decomposition studies in soil: history of the assay and development. In Cotton strip assay: an index for decomposition in soils (pp. 7–9). ITE Symposium, Institute of Terrestrial Ecology, Natural Environment Research Council, UK.
Lenth, R., & Love, J. (2018). lsmeans: least-squares means. R package version 2.27-62.
Martin, M. (2011). Cutadapt removes adapter sequences from high-throughput sequencing reads. EMBnet.Journal, 17(1), 10–12.
Meagher, M. M. (1973). The bison of Yellowstone National Park. NPS Scientific Monograph (Vol. 1). National Park Service, Yellowstone Center for Resources.
Melis, C., Selva, N., Teurlings, I., Skarpe, C., Linnell, J. D. C., & Andersen, R. (2007). Soil and vegetation nutrient response to bison carcasses in Białowieża Primeval Forest, Poland. Ecological Research, 22(5), 807–813. doi:10.1007/s11284-006-0321-4
Nikolenko, S. I., Korobeynikov, A. I., & Alekseyev, M. A. (2013). BayesHammer: Bayesian clustering for error correction in single-cell sequencing. BMC Genomics, 14(1), S7. doi:10.1186/1471-2164-14-S1-S7
Oksanen, J., Blanchet, F. G., Friendly, M., Kindt, R., Legendre, P., McGlinn, D., … Wagner, H. H. (2019). vegan: community ecology package. R package version 2.5-4.
Pinheiro, J., Bates, D., DebRoy, S., & Sarkar, D. (2018). nlme: Linear and nonlinear mixed effect models. R package version 3.1-131.1.
Quast, C., Pruesse, E., Yilmaz, P., Gerken, J., Schweer, T., Yarza, P., … Glöckner, F. O. (2013). The SILVA ribosomal RNA gene database project: improved data processing and web-based tools. Nucleic Acids Research, 41(Database issue), D590–D596. doi:10.1093/nar/gks1219
Quimby, D. C., & Johnson, D. E. (1951). Weights and measurements of Rocky Mountain elk. Journal of Wildlife Management, 15, 57–62.
R Core Team. (2017). R: A language and environment for statistical computing. R Foundation for Statistical Computing, Zurich, Switzerland.
R Core Team. (2019). R: A language and environment for statistical computing. Vienna, Austria: R Foundation for Statistical Computing.
Rime, T., Hartmann, M., Brunner, I., Widmer, F., Zeyer, J., & Frey, B. (2015). Vertical distribution of the soil microbiota along a successional gradient in a glacier forefield. Molecular Ecology, 24(5), 1091–1108. doi:10.1111/mec.13051
Risch, A. C., Jurgensen, M. F., & Frank, D. A. (2007). Effects of grazing and soil micro-climate on decomposition rates in a spatio-temporally heterogeneous grassland. Plant and Soil, 298(1–2), 191–201. doi:10.1007/s11104-007-9354-x
Schloss, P. D., Westcott, S. L., Ryabin, T., Hall, J. R., Hartmann, M., Hollister, E. B., … Weber, C. F. (2009). Introducing mothur: open-source, platform-independent, community-supported software for describing and comparing microbial communities. Applied and Environmental Microbiology, 75(23), 7537–7541. doi:10.1128/AEM.01541-09
Smith, D., Stahler, D., Cassidy, K., Stahler, E., Metz, M., Cassidy, B., … Cato, E. (2018). Yellowstone National Park wolf project annual report 2017. Yellowstone National Park, Mammoth, WY, USA: National Park Service, Yellowstone Center of Resources.
Wang, Q., Garrity, G. M., Tiedje, J. M., & Cole, J. R. (2007). Naive Bayesian classifier for rapid assignment of rRNA sequences into the new bacterial taxonomy. Applied and Environmental Microbiology, 73(16), 5261–5267. doi:10.1128/AEM.00062-07
Withington, C., & Sanford Jr., R. (2007). Decomposition rates of buried substances increase with altitude in a forest-alpine tundra ecotone. Soil Biology and Biochemistry, (39), 68–75.

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

bacteria

display_name: bacteria

biogeochemical-cycling

display_name: biogeochemical-cycling

carcass

display_name: carcass

carrion

display_name: carrion

decomposition

display_name: decomposition

detritus

display_name: detritus

fungi

display_name: fungi

soil-biodiversity

display_name: soil-biodiversity

wolf

display_name: wolf

yellowstone

display_name: yellowstone

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: Elk and bison carcasses in Yellowstone, USA


en: zurich plant-species flora-change uetliberg occurrence

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.

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

uetliberg

display_name: uetliberg

zurich

display_name: zurich

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


weissfluhjoch-dataset-for-esm-snowmip

maintainer: Nander Wever

title_for_slug: weissfluhjoch-dataset-for-esm-snowmip

en: snow-models weissfluhjoch esm-snowmip snow snow-depth

mimetype: application/zip

en: Conversion script

en:
Use this script to convert WFJ_optimaldataset_v6.smet to wfj.smet, the file that is used for the ESM-SnowMIP project. It also requires the file: WFJ_AirPressure_Data.zip

Use: bash create_wfj_dataset.sh > input/wfj.smet

mimetype: text/x-sh

en: Dataset Weissfluhjoch for ESM-SnowMIP

en: ini file

en: This ini file is required by data-converter from MeteoIO version 1887 (http://models.slf.ch/p/meteoio/)

en: This Weissfluhjoch dataset is a processed version of the Weissfluhjoch dataset version 6 from https://doi.org/10.16904/6. This dataset was specially created for the ESM-SnowMIP project. Here it is documented how this dataset has been created.

esm-snowmip

display_name: esm-snowmip

snow

display_name: snow

snow-depth

display_name: snow-depth

snow-models

display_name: snow-models

weissfluhjoch

display_name: weissfluhjoch

en: Weissfluhjoch dataset for ESM-SnowMIP


en: traits ecology dispersal reef-fish biodiversity

en: Global species distribution of tropical reef fish species

en: Each species corresponds to a "Gaspar_code" gathered from the General Approach to Species Abundance Relationships (GASPAR) database (Kulbicki et al. 2013, Parravicini et al. 2013) and is linked to a specific Fishned ID corresponding to a specific Latitude and Longitude.

en: Global simulated distribution of species under a range of dispersal parameter values

en:
Global distribution of simulated species richness under a range of dispersal parameter values d
d ∈ [1.75°: 5.45°].

mimetype: text/plain

en: Tropical reef fish trait data

en:
Species trait (i.e. adult body size, home range mobility behaviour, circadian activity and schooling) data gathered from the General Approach to Species Abundance Relationships (GASPAR) database (Kulbicki et al. 2013, Parravicini et al. 2013).

Kulbicki, M. et al. 2013. Global biogeography of reef shes: a hier- archical quantitative delineation of regions. – PLoS One 8: e81847.

Parravicini, V. et al. 2013. Global patterns and predictors of tropi- cal reef sh species richness. – Ecography 36: 1254–1262.

To complement the trait data with Pelagic Larval Duration information refer to the following publication:

Luiz, Osmar J., et al. "Adult and larval traits as determinants of geographic range size among tropical reef fishes." Proceedings of the National Academy of Sciences 110.41 (2013): 16498-16502.

In Donati et al. "A process-based model supports an association between dispersal and the prevalence of species traits in tropical reef fish assemblages" accepted in Ecography in August 2019, we used the PLD gathered from Luiz et al. 2013 as described in the methods - section "Species trait data".

en: Dispersal parameter value d per simulation starting with a minimum dispersal value, where each species is able to colonise each adjacent cell, and ending with the value of d for which all the extant habitats, including the most remote Pacific islands, have been colonised (d ∈ [1.75°: 5.45°]).

en: Main text figures

en: R Script used for figures in main text in: Donati et al. 2019: "A process-based-model supports an association between dispersal and the prevalence of species traits in tropical reef fish assemblages" accepted in Ecography, August 2019.

en: Input for the Global distribution maps for proportions of species richness for (a) simulated dispersal parameter value (b) observed dispersal-related traits

en: Geographic distribution data (species richness and proportions of high/low dispersal-related traits) on predominantly low dispersing and high dispersing species expected based on the simulations, and those where low- and high- dispersal related traits values are observed for the five investigated traits.

en: Simulated rates of speciation and extinction under a range of dispersal parameters. Net diversification rates are calculated from the difference between speciation and extinction rates. This data allows the creation of Figure A4 in Supporting information, Appendix 1.

en: Input for spatial congruence test overlap between proportions of low and high dispersal and observed low- and high- dispersal-related traits in assemblages (30-50% threshold). see Table 2.

en: Coral reef grid cells (shape, dbf, etc. files)

en:
Grid cells of 5 × 5°, corresponding to circa 555 × 555 km at the Equator (see Parravicini et al. 2013, Leprieur et al. 2016)

Parravicini, V. et al. 2013. Global patterns and predictors of tropi- cal reef sh species richness. – Ecography 36: 1254–1262.

Leprieur, F. et al. 2016. Plate tectonics drive tropical reef biodiver- sity dynamics. – Nat. Commun. 7: 11461.

en: Global coast files from https://www.ngdc.noaa.gov/mgg/shorelines/gshhs.html used in the Figures

en: Supplementary material Appendix 1 Figures illustrated in Donati et al. 2019 "A process-based-model supports an association between dispersal and the prevalence of species traits in tropical reef fish assemblages". accepted in Ecography, August 2019

en: Donati et al. main script

en:
Main script used in : Donati et al. 2019 "A process-based-model supports an association between dispersal and the prevalence of species traits in tropical reef fish assemblages"
accepted in Ecography, August 2019

en: Functions used in R scripts in: Donati et al. 2019 "A process-based-model supports an association between  # dispersal and the prevalence of species traits in tropical reef fish assemblages" accepted in Ecography, August 2019

en: Functions for Figures illustrated in Donati et al. 2019 "A process-based-model supports an association between dispersal and the prevalence of species traits in tropical reef fish assemblages" accepted in Ecography, August 2019.

en:
This dataset contains all data and R codes (R Development Core Team, https://www.R-project.org) used in the following publication: Donati GFA, Parravicini V, Leprieur F, Hagen O, Gaboriau T, Heine C, Kulbicki M, Rolland J, Salamin N, Albouy C, Pellissier L. "A process-based model supports an association between dispersal and the prevalence of species traits in tropical reef fish assemblages" accepted by Ecography in August 2019. When using this data and R scripts the above publication should be cited.

The interaction of habitat dynamics with species dispersal abilities could generate gradients
in species diversity and prevalence of life-history and ecological traits, when the latter are associated with dispersal potential. In this dataset, we use a spatial mechanistic model of speciation, extinction and dispersal, constrained by a dispersal parameter. This model allows to simulate the interplay between reef habitat dynamics over the past 140 million years and dispersal, shaping lineage diversification history and global assemblage composition of over 6000 tropical reef fish species. Global trait distribution data of tropical reef fish are used to evaluate the congruence between simulations and observations.

biodiversity

display_name: biodiversity

dispersal

display_name: dispersal

ecology

display_name: ecology

reef-fish

display_name: reef-fish

traits

display_name: traits

educ

en: Education, culture and sport

en: Simulated and observed prevalence of dispersal-related traits in tropical reef fish assemblages worldwide


maintainer: Rebecca Mott

en: patchy-snow-covers riegl-vz6000 terrestrial-laser-scanning tls snow-ablation-rates

en: Snowmask 2014

en: Snowmask 2016

en: Digital Elevation Modell 2015

en: Snowmask 2015

en: Digital Elevation Modell 2014

en: Digital Elevation Modell 2016

en: Gletschboden test site

en: We recorded snow ablation maps with a terrestrial laser scanner (TLS, Riegl-VZ6000) at the Gletschboden area. The TLS position is located approximately 30 vertical meters above the Gletschboden area at a northerly exposed slope. In total 44 TLS measurement sets have been conducted in three consecutive years 2014-2016 (2014: 13 measurements; 2015: 17 measurements; 2016: 14 measurements). The TLS system has a single-point measurement frequency of 300 kHz and a beam divergence of 0.007°. This set-up allows a horizontal resolution of approximately 0.01 m in 100 m distance to the TLS position. One scan of the Gletschboden area lasts approximately 15 minutes. The travel time from the laser scanner towards the surface is recorded and afterwards converted into a point cloud of distances. 5 reflectors located at the Gletschboden area and in the closer surroundings were additionally scanned during each measurement to transform the point cloud from the scanner own coordinate system into Swiss coordinates. Additionally, orthophotos have been created by using pictures recorded from the TLS in order to provide snow mask maps. Snow and bare ground can be distinguished by the RGB color information of the orthophoto. Cells with blue band information greater than 175 were categorized as snow and all cells with values smaller or equal 175 were categorized as bare ground.

patchy-snow-covers

display_name: patchy-snow-covers

snow-ablation-rates

display_name: snow-ablation-rates

terrestrial-laser-scanning

display_name: terrestrial-laser-scanning

tls

display_name: tls

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: DISCHMEX - High-resolution daily snow ablation rates in an Alpine environment