en: insect drone ins16s edna switzerland minion

en: Data access

en: Please use cyberduck to download

en:
Traditional methods of biodiversity monitoring are often logistically challenging, time-consuming, require experienced experts on species identification and sometimes include destruction of the targeted specimens. Here, we investigated a non-invasive approach of combining the use of drones and environmental DNA (eDNA) to monitor insect biodiversity on vegetation.
We aimed to assess the efficiency of this novel method in capturing insect diversity and comparing insect composition across different vegetation types (grassland, shrub, and forest) in Switzerland. A commercial, off-the-shelf drone was equipped with a specialised probe that autonomously swabbed vegetation and collected eDNA. Then, samples were processed using rapid third-generation Oxford Nanopore sequencing. The obtained data were analysed for insect diversity, comparing taxonomic richness, evenness and community composition across the three habitat types using statistical techniques. Sequencing of the samples yielded 76 hexapods taxa, revealing an insect community with notable differences in taxonomic richness but not in evenness across grassland, shrub, and forest habitats.
Our study demonstrates the potential of drone-based sampling integrated with eDNA and nanopore sequencing for biodiversity monitoring, offering a non-destructive method for detecting insect occurrence on plant surfaces. Integrating robotics and eDNA technology provides a promising solution for fast, large-scale, non-invasive biodiversity monitoring, potentially improving conservation efforts and ecosystem management.

drone

display_name: drone

edna

display_name: edna

insect

display_name: insect

minion

display_name: minion

switzerland

display_name: switzerland

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: Robot-aided measurement of insect diversity on vegetation using environmental DNA


disdrometer-data-gotschnagrat

maintainer: EnviDat Support

title_for_slug: disdrometer-data-gotschnagrat

en: precipitation raclets disdrometer hydrometeors visibility

state: active

type: dataset

en: Disdrometer Data Gotschnagrat

media_type: application/zip

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

format: ZIP

mimetype: application/zip

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

disdrometer

display_name: disdrometer

hydrometeors

display_name: hydrometeors

precipitation

display_name: precipitation

raclets

display_name: raclets

visibility

display_name: visibility

educ

fr: Éducation, culture et sport

de: Bildung, Kultur und Sport

en: Education, culture and sport

it: Istruzione, cultura e sport

envidat

fr: EnviDat: le portail de données environnementales

de: EnviDat: das Umwelt-Datenportal

en: EnviDat: the Environmental Data Portal

it: EnviDat: il portale dei dati ambientali

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

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

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

format: XLS

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

en: Elk and bison carcasses in Yellowstone, USA


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

en: Documentation

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

format: SERVICE

mimetype: application/msword

en: Dataset V1

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

format: GDB

en: Site photo

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

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

afforestation

display_name: afforestation

long-term-experiment

display_name: long-term-experiment

mountain-forest

display_name: mountain-forest

stillberg

display_name: stillberg

treeline

display_name: treeline

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


en: illgraben debris-flow rainfall radar surge-waves

media_type: text/csv

en: Radar-based flow height measurement of debris flow at CD28 at Illgraben. Flow height is derived relative to pre-event channel-bed elevation. Sensor location: 46.309677N, 7.633304E

format: CSV

en: Cumulative rainfall measured at CD1 in the Illgraben catchment. Sensor location: 46.283287N / 7.619689E

en:
This dataset contains measurements from two debris flows recorded in 2024 at the Illgraben debris-flow observatory in Switzerland. The first debris flow was recorded on 15 June 2024 and the second debris flow was recorden on 21 June 2024.

This dataset contains the following reseach data for both:
a) Cummulative rainfall measured at CD1 in the catchment.
b) Radar-based flow height of debris flows measured at CD28.

Abstract
In recent years, the destructive impact of debris flows in alpine regions has become increasingly evident. Surge waves within debris flows increase peak discharge and magnify the hazard potential. Hence, understanding the dynamic complexity of debris flows is crucial to mitigate their risk. In order to capture the dynamic processes involved in the formation and interaction of surge waves, it is necessary to obtain distributed observations in the spatiotemporal domain. In this study, we present near-torrent distributed seismic measurements to monitor the Illgraben channel located in the Swiss Alps. With 33 nodal sensors, we detected and tracked surge waves along a 2-kilometer torrent section across the Illgraben fan, which allowed us to gain valuable new insights into the spatial scales relevant for surge wave formation and their long-distance propagation characteristics. We observed erosion-deposition waves that emerged out of the muddy flow tail and propagated with constant velocity along the torrent, reaching meter-scale flow heights within only 100s of meters of flow distance which significantly impact the hazard potential of debris flows. Our results provide valuable observations of surge waves from their formation to their annihilation. We can differentiate flow regimes based on their seismic signature and track them along the torrent, thus mapping the debris-flow evolution in time and space. The observations elucidate large-scale debris flow dynamics thus improving our understanding of hazard potential and the effectiveness of structural countermeasures.

debris-flow

display_name: debris-flow

illgraben

display_name: illgraben

radar

display_name: radar

rainfall

display_name: rainfall

surge-waves

display_name: surge-waves

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: Debris flow observation at Illgraben 2024: Event Data 15 June / 21 June


chelsacanaryclim-climatologies

title_for_slug: chelsacanaryclim-climatologies

en: climate climatologies air-temperature canaries precipitation

en:
Precipitation
Files are provided as Cloud-Optimized GeoTIFFs (COGs) with standardized metadata.
Each COG encodes scale and offset parameters in its metadata. Standards-compliant software will apply these fields automatically and return values in the correct units; however, legacy or non-compliant applications may not. If there is any uncertainty regarding units, please consult the file metadata to verify the applied scale/offset and units.

en: CHELSACanaryClim-climatologies: Daily Mean Near-Surface Air Temperature

en:
Daily Mean Near-Surface Air Temperature
Files are provided as Cloud-Optimized GeoTIFFs (COGs) with standardized metadata.
Each COG encodes scale and offset parameters in its metadata. Standards-compliant software will apply these fields automatically and return values in the correct units; however, legacy or non-compliant applications may not. If there is any uncertainty regarding units, please consult the file metadata to verify the applied scale/offset and units.

en: CHELSACanaryClim-climatologies: Daily Maximum Near-Surface Air Temperature

en:
Daily Maximum Near-Surface Air Temperature
Files are provided as Cloud-Optimized GeoTIFFs (COGs) with standardized metadata.
Each COG encodes scale and offset parameters in its metadata. Standards-compliant software will apply these fields automatically and return values in the correct units; however, legacy or non-compliant applications may not. If there is any uncertainty regarding units, please consult the file metadata to verify the applied scale/offset and units.

en: CHELSACanaryClim-climatologies: Daily Minimum Near-Surface Air Temperature

en:
Daily Minimum Near-Surface Air Temperature
Files are provided as Cloud-Optimized GeoTIFFs (COGs) with standardized metadata.
Each COG encodes scale and offset parameters in its metadata. Standards-compliant software will apply these fields automatically and return values in the correct units; however, legacy or non-compliant applications may not. If there is any uncertainty regarding units, please consult the file metadata to verify the applied scale/offset and units.

en:
CHELSACanaryClim is a high-resolution, terrain-informed downscaling model developed specifically for the Canary Islands. It builds on the CHELSA v1.2 framework and integrates extensive local meteorological station data to refine temperature and precipitation estimates. The model incorporates high-resolution elevation data (down to 5 m), planetary boundary layer height, and ERA-Interim reanalysis inputs to simulate fine-scale climatic variation in mountainous island terrain.
CHELSACanaryClim-climatologies is a very-high resolution climate dataset generated with the CHELSACanaryClim downscaling model. It consists of monthly climatologies of air-temperatures and precipitation.

air-temperature

display_name: air-temperature

canaries

display_name: canaries

climate

display_name: climate

climatologies

display_name: climatologies

precipitation

display_name: precipitation

educ

en: Education, culture and sport

en: EnviDat: the Environmental Data Portal

en: CHELSACanaryClim-climatologies


figures-perspective-urban-beekeeping

maintainer: Joan Casanelles

title_for_slug: figures-perspective-urban-beekeeping

en: diversity-distributions insects hymenoptera wildbees urban-beekeeping urban-ecology

en: DEPRECATED. Data growth urban beekeeping

en: R script for the figures V1

en: Deprecated version of the R script

format: OCTET

en: R script for the figures V2

en: R script for the figures

en: Data growth urban beekeeping

en:
The dataset contains the data of the growth of urban beekeeping in different cities.
For each city in a given year, it contains the following:
Continent.
Country.
City: the name of the city
Year: the year when the information was collected
Area: of the city
Total N. beekeepers: when available, the estimated number of beekeepers in that city for that given year
Total N. hives: when available, the estimated number of beehives in that city for that given year
Density: the total number of hives divided by the city area
Reference: the source of the information.

en: DEPRECATED. Distirbution beehives among beekeepers

en: The dataset contains the number of beehives per registered beekeeper ID (annonymised) in four Swiss cities (Bern, Lausanne, Geneve, Zurich).

en: Results literature review

en:
 The file shows the results from the literature review. Briefly, we searched papers using google scholar search engine using the following query: (“WILD BEE OR WILDBEE”)(“URBAN” OR “CITY”), and limited the time span from 2010-2023. The search query returned 200 candidate papers. In addition, we complemented the candidate papers from the literature research performed by Ferrari & Polidori (2022), adding 22 additional candidate papers. To select papers, we checked that (1) were conducted in urban areas; (2) sampled the whole bee community; (3) provided data on abundance of wildbees; (4) provided data on honeybees; and (5) provided individual abundance data of each wild bee species.
The dataset contains the following:
-Article_ID: ID for the specific article in the form "A1", "A2"..."An"
- Title: of the article
- Year: of publication
- Journal: of publication
- Publisher:
- Link: link to the publication
- DOI: when applicable
- Total abundance wild bees reported: was the total number of collected bees reported? Logical (Y/N)
- Honey bee abundance reported: was thenumber of honeybees collected reported? 	Logical (Y/N)
- Abundance per wild bee species: was the number of wildbee species sampled provided? Logical (Y/N)
- Select proportion: paper selected to calculate the proportion of honeybees and wildbees.
- Select RAD: paper selected to compute the rank-abundance distribution diagram
Comment: comments on the papers, data availability, etc.

en: Coordinates studied cities

en: Coordinates (LatLon format) of the cities where data from urban bee ecology studies was used.

en: NDVI values within 3 buffers  in hives in Zurich

en:
The dataset contains the average NDVI values around beehives in Zurich at three spatial scales (250, 500 and 1000 m). It contains 3 columns_
- buffer: indicating the spatial scale
- ID: hive ID (annonymised)
- mean.NDVI: mean NDVI value

en: Data rank-abundance distribution urban bees

en: Outdated, use the new resource

en: Local overheating values within 3 buffers in hives in Zurich

en:
The dataset contains the average overheating values around beehives in Zurich at three spatial scales (250, 500 and 1000 m). It contains 4 columns:
- buffer: indicating the spatial scale
-ID: hive ID (annonymised)
- mean.overwarming: mean overheating value, expressed in degrees Kelvin
-mena.overwarming.cor = transformed values do degrees Celsius

en: Proportion honeybees and wildbees

en: Outdated, use the new resource "Propotion urban honeybees and wildbees"

en: Proportion urban honeybees and wildbees

en:
The dataset contains the proportion of wildbees and honeybees in the different studies obtained from the literature review.
Article_ID: ID for each article
DOI
Authors
Year: publication year
Duration sampling (years): numerical
Start_sampling: numerical, date
End_sampling: numerical, date
Continent
Country
N. cities: number of cities sampled in the article. Numerical.
City
Sampling type: categorical. Levels: active (e.g., Hand-netting); passive (e.g., pantraps. trap-nests); both (combination of passive and active methods).
Sampling methodology: categorical. Levels: direct observations, hand-netting, pantraps, interception traps, vane traps.
Number sites: total number of study sites.
Abundance honeybees: number of honeybees recorded
Abundance wild bees: number of wildbees recorded
Total bees: total number of bees recorded.
Proportion honeybees: Abundance of honeybees / Total number of bees
Proportion wildbees: Abundance of wildbees / Total number of bees

en: Species-abundance data

en:
Abundance data at the species level per used dataset for the rank abundance distribution (RAD).
40 datasets used.

en: Distribution beehives among beekeepers

en: The dataset contains the number of beehives per registered beekeeper ID (annonymised) in four Swiss cities (Bern, Lausanne, Geneve, Zurich) and Paris.

en:
Data and code from the perspective paper "When honeybees comes to town"
The .r file provides the code to generate the figures.
In addition, this repository contains the data for the figures 1-3.
For Figure 4, part of the data is confidential, Please, refer to the contacts provided:
- For the distribution of hives in Zurich (2018): https://www.zh.ch/de/gesundheitsdirektion/veterinaeramt.html
- For the overheating map of Zurich: Prof. Dr. Eberhard Parlow / Stadt Zurich (https://www.zh.ch/de/umwelt-tiere/umweltschutz/umweltpraxis/definitionsseite/2012/68/zup068_2012_a0030_klimaanalyse-pdf.html)

diversity-distributions

display_name: diversity-distributions

hymenoptera

display_name: hymenoptera

insects

display_name: insects

urban-beekeeping

display_name: urban-beekeeping

urban-ecology

display_name: urban-ecology

wildbees

display_name: wildbees


en: spatial-modelling land-use-and-cover-change topography built-up-classification forest-gain planning-outcome forest-persistence nature-conservation urban-morphology basic-services urban-compactness urban-sprawl

en: Increase in clean water provision service

format: GeoTIFF

en: Permanent housing density increase

en: slope

en: Slope °

en: Urban persistence: Built-up 2005 = Built-up 2015

en: Ecological-Economic Zoning (EEZ)

format: SHP

en: Population density per pixel (change per year)

en: Native forest cover gains from 2005 to 2015

en: Human Development Index (HDI) per municipality (change per year)

en: Master plan Ubatuba (zones)

en: Mean income in Reais (R$) per census sector (change per year)

en: Descricao dos dados em portiuguês

media_type: application/pdf

en: Portugues description

format: PDF

en: Increase in Normalized Difference Vegetation Index

en: infill

en: New built-up pixels classified as infill

en: Native forest cover persistence from 2005 to 2015

en: Topographic Index Position (TPI)

en: isolated

en: New built-up pixels classified as isolated

en: Axial

en: New built-up pixels classified as axial

en: Variables description

en: Table of content. Variables description, source, and other important information

en: Increase in waste collection service

en:
Basic education in % per census sector (change per
year)

en: Master plan Ihabela (zones)

en: Increase in sanitation service

en:
The present dataset is part of the published scientific paper entitled “The role of spatial planning in land change: An assessment of urban planning and nature conservation efficiency at the southeastern coast of Brazil” (Pierri Daunt, Inostroza and Hersperger, 2021). In this work, we evaluated the conformance of stated spatial planning goals and the outcomes in terms of urban compactness, basic services and housing provision, and nature conservation for different land-use strategies. We evaluate the 2005 Ecological-Economic Zoning (EEZ) and two municipal master plans from 2006 in a coastal region in São Paulo State, Brazil. We used Partial Least Squares Path Modelling (PLS-PM) to explain the relationship between the plan strategies and land-use change ten years after implementation in terms of urban compactness, basic services and housing increase, and nature conservation.

We acquired the data for the explanatory variables from different sources listed on Table 1. Since the model is spatially explicit, all input data were transformed to a 30 m resolution raster. Regarding the evaluated spatial plans, we acquired the zones limits from the São Paulo State Environmental Planning Division (CPLA-SP), Ilhabela and Ubatuba municipality.

1)	Land use and cover data: Urban persistence, Urban axial, Urban infill, Urban Isolates, Forest cover persistence, Forest cover gain, NDVI increase

We acquired two Landsat Collection 1 Higher-Level Surface Reflectance images distributed by the U.S. Geological Survey (USGS), covering the entire study area (paths 76 and 77, row 220, WRS-2 reference system, https://earthexplorer.usgs.gov/). We classified one image acquired by the Landsat 5 Thematic Mapper (TM) sensor on 2005-05-150, and one image from the Landsat 8 Operational Land Imager (OLI) sensor from 2015-08-15. We collected 100 samples for forest cover, 100 samples for built-up cover and 100 samples for other classes. We then classified these three classes of land cover at each image date using the Support Vector Machine (SVM) supervised algorithm (Hsu et al., 2003), using ENVI 5.0 software.

Land-use and land-cover changes from 2005 to 2015 were quantified using map algebra, by mathematically adding them together in pairs (10*LULC2015 + LULC2005). We reclassified the LULC data into forest gain (conversion of any 2005 LULC to forest cover in 2015); forest persistence (2005 forested pixels that remained forested in 2015); new built-up area (conversion of any 2005 LULC to built-up in 2015); and urban maintenance (2005 built-up pixels that remained built-up in 2015).

To describe the spatial configuration of the urban expansion, we classified the new built-up areas into axial, infill and isolated, following Inostroza et al. (2013) (For details, please refer to Supplementary Material I at the original publication).

The NDVI was obtained from the same source used for the LULC data. With the Google Engine platform, we used an annual average for the best pixels (without clouds) for 2005 and 2015, and we calculated the changes between dates. We used increases of > 0.2 NDVI to represent an improvement in forest quality.

2)	Federal Census data organization: Urban Basic Services and Housing indicator, socioeconomic and population:

The data used to infer the values of basic services provision, socioeconomic and population drivers was derived from the Brazilian National Census data (IBGE, 2000 and 2010). Population density, permanent housing unit density, mean income, basic education, and the percentage of houses receiving waste collection, sanitation and water provision services, called basic services in the context of this study, were calculated per 30 m pixel. The Human Development Index is only available at the municipality level. We attributed the HDI for the vector file with the municipality border, and we rasterized (30 m resolution) this file in QGIS. Annual rates of change were then calculated to allow comparability between LULC periods. To infer the BSH, we used only areas with an increase in permanent housing density and basic services provision (See Supplementary Material I at the original publication).

3)	Topographic drivers

To infer the values of the topographic driver, we used the slope data and the Topographic Index Position (TPI) based on the digital elevation model from SRTM (30 m resolution) produced by ALOS (freely available at eorc.jaxa.jp/ALOS/en/about/about_index.htm), and both variables were considered constant from 2005 to 2015 (See Supplementary Material I at the original publication).

basic-services

display_name: basic-services

built-up-classification

display_name: built-up-classification

forest-gain

display_name: forest-gain

forest-persistence

display_name: forest-persistence

land-use-and-cover-change

display_name: land-use-and-cover-change

nature-conservation

display_name: nature-conservation

planning-outcome

display_name: planning-outcome

spatial-modelling

display_name: spatial-modelling

topography

display_name: topography

urban-compactness

display_name: urban-compactness

urban-morphology

display_name: urban-morphology

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: Spatially explicit data to evaluate spatial planning outcomes in a coastal region in São Paulo State, Brazil


maintainer: Alexandre Buttler

en: climate-change biogeochemisty transplantation-experiment silvopastoral-systems soil

en: Dataset

en: Zip archive of all datasets detailed in study.

en:
Silvopastoral systems are highly productive and combine long-term wood production with annual provision of forage for livestock. In the Swiss Jura Mountains these systems are a key component of the landscape. As in other cold biomes, climate change can potentially accelerate landscape change within these historically sustainable systems.

In order to anticipate the evolution of subalpine wooded pasture ecosystems under future climate and land-use changes, this project focused on the interplay between soil, vegetation and climate. It was aimed at providing experimental evidence for chief ecosystem processes, with emphasis on the quality of the ecosystem services provided. The main interest was placed on vegetation turf resistance to climate change along an unwooded – sparsely wooded - densely wooded pasture gradient (land-use intensity), where plant productivity, diversity and succession along with rates of carbon cycling and microbial activity provided measures of ecosystem functioning at both plot and landscape level.

Experimental transplantation of monolith soil turfs to lower altitudes allowed to simulate soil warming and reduced annual precipitation. In order to simulate a year-round warmer and drier climate the natural climate variation along an altitudinal gradient was used as a proxy. The aim was to simulate realistic climate change scenarios for the second half of the 21st century predicted by the IPCC report and downscaled for Switzerland providing regionalized interpolated projections integrating therein trends for temperature increase and precipitation decrease. By using permanent meteorological stations within the network of the Federal Office of Meteorology and Climatology (MeteoSwiss), we obtained high resolution regional data on the variation of mean annual temperature (MAT) and mean annual precipitation (MAP) in relation to altitude in the Swiss Jura Mountains. We observed a general increase of +0.5 K in MAT and a decrease of -20 % MAP for each 100 m decrease in altitude along the SE slope of the Swiss Jura Mountains. These relationships served for the selection of the transplantation sites such that in comparison to a control site at 1350 m a.s.l. (Combe des Amburnex, N 46°54’, E 6°23’) a +2 K MAT and -20 % MAP was achieved at 1010 m a.s.l. (Saint-George, N 46°52’, E 6°26’), a +4 K MAT and -40 % MAP at 570 m a.s.l., (Arboretum d’Aubonne, N 46°51’, E 6°37’), and a +5 K MAT and -50 % MAP at 395 m a.s.l. (Les Bois Chamblard, N 46°47’, E 6°41’). The two stations at 1010 m a.s.l. and 570 m a.s.l. corresponded to the IPCC scenario A1B for a moderate increase in greenhouse gas emissions and to scenario A2 for a high increase in greenhouse gas emissions, respectively. The station at 395 m a.s.l. was chosen to represent an extreme scenario with climate variables lying at the positive tail distribution of model predictions under the A2 scenario.

Soil cores were assembled into rectangular PVC boxes of 60  80 cm2 size and of 35 cm height. All mesocosms were dug down to surface level into previously prepared trenches in the ground thus preventing lateral heat exchange with the atmosphere. Since at each site the mesocosms were placed in a common garden with no light interception, mesocosms with turfs from the two wooded pastures were shaded from direct sun light to simulate the natural light conditions in the corresponding habitats. Each mesocosm was equipped with a drainage system and was connected to a water tank thus representing a zero potential lysimeter collecting soil solution and precipitation/snowmelt runoff. ECH2O EC-TM sensor probes coupled to Em50 data-loggers (Decagon Devices, Inc., USA) recorded soil temperature and volumetric water content in each mesocosm at the top-soil (0 to -3 cm) every minute and data were averaged over one hour intervals. Climate parameters at each transplantation site were monitored continuously throughout the experiment by means of automated weather stations (Sensor Scope Sàrl, Switzerland), measuring rain precipitation (non-heated tipping bucket gauges) and air temperature and humidity 2 m above the ground surface at one minute intervals.

A list of above- and belowground variables were measured to assess the resilience of biogeochemical processes, plant productivity, tree regeneration, and carbon sequestration for each respective land-use practice. Furthermore, the experimental data were used to improve on (parameterization) the existing spatially explicit, dynamic model WoodPaM and refine the modelʼs climatic and land-use variables so that different scenarios of climate change and land use change could be simulated. Natural and management induced disturbance patterns were incorporated into the model.
The data have been made available within the project CCES Mounted. The climate stations Sensorscope are still in use within the project CLIMARBRE (Wald und Klimawandel, WSL/BAFU).

#References

1. Puissant, J., Cécillon, L., Mills, R.T.E., Robroek, B.J.M. Gavazov, K., De Danieli, S., Spiegelberger, T., Buttler, A., Brun, J.J. 2015. Seasonal influence of climate manipulation on microbial community structure and function in mountain soils. Soil Biology and Biochemistry 80: 296–305.
2. Mills, R., K. Gavazov, T. Spiegelberger, D. Johnson and A. Buttler 2014. Diminished soil functions occur under simulated climate change in a sup-alpine pasture, but heterotrophic temperature sensitivity indicates microbial resilience. Science of the Total Environment, vol. 473–474(0): 465-472.
3. Gavazov, K., Spiegelberger, T. and Buttler, A. 2014. Transplantation of subalpine wood-pasture turfs along a natural climatic gradient reveals lower resistance of unwooded pastures to climate change compared to wooded ones. Oecologia (174) : 1425-1435.
4. Peringer A., Siehoff S., Chételat J., Spiegelberger T., Buttler A. & Gillet F. 2013. Past and future landscape dynamics in pasture-woodlands of the Swiss Jura Mountains under climate change. Ecology and Society, 18, 3: 11. DOI: 10.5751/ES-05600-180311. [online] URL: http://www.ecologyandsociety.org/vol18/iss3/art11/
5. Gavazov, K. S., A. Peringer, A. Buttler, F. Gillet and T. Spiegelberger. 2013. Dynamics of Forage Production in Pasture-woodlands of the Swiss Jura Mountains under Projected Climate Change Scenarios. Ecology and Society 18 (1): 38. [online] URL: http://www.ecologyandsociety.org/vol18/iss1/art38/

biogeochemisty

display_name: biogeochemisty

climate-change

display_name: climate-change

silvopastoral-systems

display_name: silvopastoral-systems

soil

display_name: soil

transplantation-experiment

display_name: transplantation-experiment

educ

en: Education, culture and sport

en: EnviDat: the Environmental Data Portal

en: Biogeochemical data from a transplantation experiment of monolith soil turfs along an altitudinal gradient to simulate climate change scenarios


en: piloderma-croceum cenococcum-geophilum ectomycorrhiza quercus-robur oak rhythmic-growth

en:
Contains growth stage data assessed over the experimental period.
Columns:
- ID = Tree identifier.
- Set = Date of plant preparation.
- Treatment = Experimental treatment.
- Date = Date of growth stage assessment,
- Days = Number of past days since start of experiment.
- Stage = Growth stage (XY = Groth cycle & development stage).
- Week = Experimental week.

en:
Contains phenotypic data assessed during the destructive sampling step of the experiment.
Columns:
- ID = Tree identifier.
- Treatment = Experimental treatment.
- nSF = Number of completed shoot flushes.
- Max_Stages_Reached = Total number of growth stages reached during the experiment.
- n_L_SF1 = Number of leaves of the second newest shoot flush at time of sampling.
- n_L_SF2 = Number of leaves of the newest shoot flush at time of sampling.
- Alive = Plant alive or not.
- Contamination = Plant contaminated or not.
- Exclude = Exclude plant or not.
- Shoot_Length_Init = Shoot length at start of the experiment.
- Shoot_Length = Shoot length at sampling.
- Delta_Length = Shoot length increase during experiment.
- FW_Plant = Fresh weight total plant.
- DW_Plant = Dry weight total plant.
- FW_Shoot = Fresh weight shoot.
- DW_Shoot = Dry weight shoot.
- FW_Stem = Fresh weight stem.
- DW_Stem = Dry weight stem.
- FW_L_SF1 = Fresh weight leaves second newest shoot flush.
- DW_L_SF1 = Dry weight leaves second newest shoot flush.
- FW_L_SF2 = Fresh weight leaves newest shoot flush.
- DW_L_SF2 = Dry weight leaves newest shoot flush.
- FW_L_Rest = Fresh weight remaining leaves.
- DW_L_Rest = Dry weight remaining leaves.
- FW_Bud = Fresh weight bud.
- DW_Bud = Dry weight bud.
- FW_Roots_Total = Fresh weight total roots.
- DW_Roots_Total = Dry weight total roots.
- FW_PR = Fresh weight principal roots.
- DW_PR = Dry weight principal roots.
- FW_LR = Fresh weight lateral roots.
- DW_LR = Dry weight lateral roots.
- A_L_SF1 = Leave area second newest shoot flush.
- A_L_SF2 = Leave area newest shoot flush.
- N_Ceno = Number of root tips mycorrhized by *Cenococcum geophilum*.
- N_Pilo = Number of root tips mycorrhized by *Piloderma croceum*.
- N_Other = Number of root tips mycorrhized by other species.
- N_No = Number of not mycorrhized root tips.
- Length_Tot = Total root length.
- Area_Tot = Total root surface area.
- Diameter_Avg = Average root diameter.
- Root_Vol = Total root volume.
- Tips = Total number root tips.
- Forks = Total number root forks.
- Crossings = Total number root crossings.
- Length_Fine = Root length fine roots (diameter < 1mm).
- SA_Fine = Surface area fine roots (diameter < 1mm).
- Vol_Fine = Volume fine roots (diameter < 1mm).

en:
In this experiment, we investigated the inoculation-effects of two ectomycorrhizal fungi (EMF) species with contrasting evolutionary histories, ecological properties, host-preferences, and habitat-ranges on phenotypic responses and growth dynamics of pedunculate oak (*Quercus robur*), an ecologically and economically important temperate forest tree species.

We set up the mycorrhization experiment using 96 plants of a genetically uniform *Q. robur* clone (DF159) and applied four treatments: A control treatment; an inoculation-treatment with the cosmopolitan Ascomycete *Cenococcum geophilum*, which is commonly found in oak forests; an inoculation-treatment with the Basidiomycete *Piloderma croceum*, which has not yet been found in natural oak forests but has been shown in previous experiments to support oak growth; and a co-inoculation treatment. We then assessed growth stage development of the trees over eight experimental weeks and measured various phenotypic traits during a destructive sampling.

cenococcum-geophilum

display_name: cenococcum-geophilum

ectomycorrhiza

display_name: ectomycorrhiza

oak

display_name: oak

piloderma-croceum

display_name: piloderma-croceum

quercus-robur

display_name: quercus-robur

rhythmic-growth

display_name: rhythmic-growth

en: Phenotypic and Growth Stage Development Data of a Quercus robur Mycorrhization Experiment


snow-depth-mapping

maintainer: Mauro Marty

title_for_slug: snow-depth-mapping

en: avalanche snow-hydrology dsm aerial-imagery snow-water-equivalent snow-depth image-matching

en: Snow depth map 20160126

media_type: image/tiff

en:
Snow depth map generated from ADS 100 imagery (CIR). GSD of imagery = 0.16 m
Because of very diffuse light conditions at time of image acquisition the quality of the resulting snow depth values are in some regions quite poor.

format: TIFF

mimetype: image/tiff

mimetype: application/pdf

en: Snow depth map 20150415

en: Snow depth map 20160420

en: Snow depth map 20140417

en: Snow depth map generated from ADS 100 imagery (CIR). GSD of imagery = 0.18 m

en: Snow depth map 20130415

en: Snow depth map generated from ADS 80 imagery (CIR). GSD of imagery = 0.25 m

en: Snow depth map 20160309

en: Snow depth map 20100416

en: Snow depth map 20120320

en:
The available datasets are snow depth maps with a spatial resolution of 2m generated from image matching of ADS 80/100 data. Image acquisition took place at peak of winter (time when the thickest snowpack is expected). The snow depth maps are the difference of a summer DSM from the winter DSM of the corresponding date . The summer DSM used is a product of image matching of ADS 80 data from summer 2013. In the available products buildings, vegetation and outliers were masked (set to NoData).
For the elimination of buildings the TLM layer (swisstopo) was used, because this layer might not represent exactly the
state of infrastructure at time of image acquisition, it is possible that mainly in dense settlement some buildings were not successfully masked. For the relevant area above treeline the masking of buildings showed good results. Vegetation got masked for a height above ground > 1m and was detected in a combination of summer and winter data sets. As Outliers were considered unrealistic snow depths caused by a failure of the image matching algorithm. Snow depths > 15m and smaller than < -15m were classified as outliers. Negative snow depth were kept, because of an uncertainty in image orientation accuracy. It is expected that in regions with negative snow depth also positive snow depth are underestimated by the same amount, which means that an estimation of snow volume should be carried out summing up the absolute values of snow depth (also the negative ones). For volume estimation in small regions the user has to take into account, that orientation accuracy of the images is roughly around 1-2 GSD (30cm), which propagates directly to the snow depth product. Areas which are not covered by snow got assigned a value of 0 as snow depth.

The work is published in:

Bühler, Y.; Marty, M.; Egli, L.; Veitinger, J.; Jonas, T.; Thee, P.; Ginzler, C., (2015). Snow depth mapping in high-alpine catchments using digital photogrammetry. Cryosphere, 9 (1), 229-243. doi: 10.5194/tc-9-229-2015

aerial-imagery

display_name: aerial-imagery

avalanche

display_name: avalanche

dsm

display_name: dsm

image-matching

display_name: image-matching

snow-depth

display_name: snow-depth

snow-hydrology

display_name: snow-hydrology

snow-water-equivalent

display_name: snow-water-equivalent


maintainer: Océane Hames

en: arctic-sea-ice snow-deposition snow-transport mosaic antarctica openfoam

en: Neumayer III simulations

en:
Snow distribution results around Neumayer Station III obtained for the sensitivity analysis and comparison to measurements. The file contains several sub-folders, namely:
-COMP: simulation output for the comparison to measurements;
-FLOW: simulation output for the study of wind forcing impact;
-simulation_exampleCase: example case of a snowBedFoam simulation with the reference Neumayer Station mesh;
-SNOW: simulation output for the study of snow properties impact;
-STRUCT: simulation output for the study of structure properties impact.

en:
OpenFOAM-5.0 scripts containing the implemented Eulerian-Lagrangian snow transport model.
The code file provided here is not updated. The most recent version of the script can be found on the WSL/SLF GitLab repository: https://gitlabext.wsl.ch/atmospheric-models/snowbedfoam-v1-0.git

en: Paper Draft

en: This is the initial draft of the paper where the snowBedFoam 1.0. results are tested against Terrestrial Laser Scan (TLS) measurements of snow dynamics on Arctic sea ice (MOSAiC expedition). It highlights the numerical limitations of our model as well as the measurement uncertainties, which may occur in such extreme environments.

en: MOSAiC Met City preliminary (Level 2) wind data

en:
Extract from the preliminary MOSAiC atmospheric data (Level 2) for the time period 6th to 13th of November, 2019.
This data was used to set up the fluid forcing parameters in the snowBedFoam simulations on MOSAiC sea ice. It is being published in this repository with the kind permission from Matthew Shupe and his team.
The final processed and quality controlled version of this dataset (Level 3) has not been published yet. A complete reference will be added in this description once it is released.

en: Snowdrift measurements around Neumayer Station III

en: Files containing the topographical data barometrically measured in June 2009 around the German Antarctic Research station Neumayer III. Those measurements are compared to the snowBedFoam simulations to assess the ability of the model to reproduce real snow distribution observations.

en:
OpenFOAM-2.3.0. scripts containing the implemented Eulerian-Lagrangian snow transport model.

The code file provided here is not updated. The most recent version of the script can be found on the WSL/SLF GitLab repository: https://gitlabext.wsl.ch/atmospheric-models/snowbedfoam-v1-0.git

en:
snowBedFoam 1.0. is a snow transport solver implemented in the computational fluid dynamics software OpenFOAM. It is adapted from the standard multi-phase flow solver DPMFoam for application in snow-influenced environments.
To simulate aeolian snow transport, snowBedFoam 1.0. handles coupled Eulerian–Lagrangian phases, which involve a finite number of particles (snow) spread in a continuous phase (air). The snow erosion and deposition are modelled through physics-based equations similar to the ones employed in the well-established LES-Lagrangian Stochastic Model (Comola and Lehning, 2017 ; Sharma et al., 2018 ; Melo et al., 2022). This modelling approach is computationally intensive and thus adapted to simulate snow movement and distribution on small scale terrain.
First, snowBedFoam 1.0. was applied to topographical data collected on Arctic sea ice during the MOSAiC expedition (Clemens-Sewall, 2021). Together with atmospheric data from the MOSAiC Met City (Shupe et al., 2021) used for the fluid forcing, the model was able to accurately simulate the zones of erosion and deposition of snow along a complex ice ridge structure (Hames et al., 2022).
Second, snowBedFoam 1.0. was used to simulate the snow distribution around the German Antarctic research station Neumayer Station III. The effect of snow properties, fluid forcing and aerodynamic structures on the snow accumulation were assessed.
snowBedFoam 1.0 was implemented in 2 different OpenFOAM versions, namely OpenFOAM-2.3.0 and OpenFOAM-5.0. The latter offers more options for turbulence models and boundary conditions. The fundamental model equations were not changed from one implementation to the other, thus both still correspond to snowBedFoam 1.0. The two branches are called snowBedFoam-v1-2.3.0 (OpenFOAM-2.3.0) and snowBedFoam-v1-5.0 (OpenFOAM-5.0). The core codes of snowBedFoam 1.0. are directly accessible on the WSL/SLF GitLab repository (more details in the Resources section).

antarctica

display_name: antarctica

arctic-sea-ice

display_name: arctic-sea-ice

mosaic

display_name: mosaic

openfoam

display_name: openfoam

snow-deposition

display_name: snow-deposition

snow-transport

display_name: snow-transport

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: snowBedFoam: an OpenFOAM Eulerian-Lagrangian solver for modelling snow transport


en: soil-biodiversity invasive-species grassland herbivory ecosystem-functioning

en: PICRUSt2 derived functional profiles of bacterial communities

media_type: text/plain

en: ASV table of fungal communities. Each column is a sampling site

format: TXT

en: ASV table of nematode communities

en: Metadata and treatment information for each of the sampling sites

en: FunGuildR derived ecological profiles of fungal communities

en: Earthworms counts and biomass for each sampling site

en: Summary table of pitfall-trap collected invertebrates.

en: ASV table of 16s (bacteria) communities. Columns are sampling sites, rows ASVs

en: PICRUSt2 derived inferred pathways for bacterial communities

en: Summary of collected biomass data. Each row is the average of 2 20 by 100 cm strips.

en: Summary of chemical and physical parameters. Each row is a sampling site

en: Summary counts and moisture adjustments for Baermann extracted nematode samples

en: Summary of sensor-collected soil moisture and temperature data

en:
Dataset supporting the paper "Herbivory mediates the response of below-ground food-webs to invasive grasses", published in the Journal of Animal Ecology.
The dataset refers to samples collected across 6 farms in the Bega Valley region of Australia. The farms are located in the grassy woodland ecoregion and are extensively managed with sheep and cattle grazing. Livestock shares the landscape with native mammalian and invertebrate herbivores. On each farm, two nested fenced exclosure systems were established. These included an open area, a fence excluding livestock but allowing access to native mammals and invertebrates, a fence excluding all mammals but allowing access to invertebrates and a shielded cage excluding all invertebrate herbivores as well. In each farm, one of these systems was located in a zone dominated by the native Kangaroo grass, and another in a zone co-dominated by the Invasive African lovegrass. The sample and treatment numbering is provided in the file Sample_metadata.
Soil samples were taken and DNA was extracted and amplified for 16s and ITS markers. The resulting metabarcoding derived ASV tables are presented (16s_ASV_table and ITS_ASV_table), as are the inferred functional profiles for bacteria at the enzyme and pathway level (16s_picrust_enzymes and 16s_picrust_pathways), as derived by the PICRUSt2 pipeline, and the fungal guilds reconstructed with FunGuildR (FunguildR_output).
Chemical, physical and enzymatic assays were also performed on the soil samples (Chemical_data).
Nematodes were extracted from soil cores with a Baermann funnel, counted (Nematodes_counts) and had their DNA extracted and amplified (Nematodes_asv_table). Soil invertebrates were sampled with below-ground pitfall traps and identified to family level (Invertebrates) and earthworms were manually extracted from 20*20*20 cm monoliths ((Earthworm_counts).
Two 20 by 100 cm strips had their vegetation removed and their living and litter biomass quantified by dry weight (Biomass_summary). Sensors measuring moisture and temperature 10 cm beneath the soil surface were installed in each plot and their output is presented in Microclimate_summary.

ecosystem-functioning

display_name: ecosystem-functioning

grassland

display_name: grassland

herbivory

display_name: herbivory

invasive-species

display_name: invasive-species

soil-biodiversity

display_name: soil-biodiversity


greenland-shrubs-and-microclimate

maintainer: Nathalie Chardon

title_for_slug: greenland-shrubs-and-microclimate

en: climate field-data accessible-shrub-forest arctic sdm validation

en: Kangerluarsunnguaq

en:
 Collected August 2020 (PI: Nathalie Isabelle Chardon)

These data collected August 2020 (PI: Nathalie Isabelle Chardon). Please contact N. I. Chardon (nathalie.chardon_at_gmail.com) for individual quadrat (i.e. 1 m x 1 m) data, which are averaged at the 90 m spatial grid here.

 COLUMN ABBREVIATIONS

 Metadata for 90 m spatial grid

id: sampling zone and unique 90 m grid identifier

long: WGS84 longitude

lat: WGS84 latitude

x_stere: longitude in Polar Stereographic (EPSG 4326)

y_stere: latitude in Polar Stereographic (EPSG 4326)

date: sampling day.month.year

 Species presence [1] or absence [0] at grid level

alcr: _Alnus crispa_

bena: _Betula nana_

dila: _Diapensia lapponica_

emni: _Empetrum nigrum_

hahy: _Harimanella hypoides_

lopr: _Loiseleuria procumbens_

oxpa: _Oxycoccus palustre_

phca: _Phyllodoce caerulea_

rhod: _Rhododendron_ sp.

saar: _Salix arctica_

sagl: _Salix glauca_

sahe: _Salix herbacea_

vaul: _Vaccinium uliginosum_

drin: _Dryas integrifolia_

thpr: _Thymus praecox_

 Habitat characteristics [% cover]

shrub: all shrub species

gram: graminoids

forb: forbs

bryo: bryophytes

lich: lichens

litt: litter

bare: bare ground

stone: stones (> 2 cm)

org: organic crust

 Shrub species height (maximum vegetative height) [mm] and cover (estimated in 1x1 m quadrat) [%]

alcr_c: _Alnus crispa_ cover

alcr_h: _Alnus crispa_ height

bena_c: _Betula nana_ cover

bena_h: _Betula nana_ height

dila_c: _Diapensia lapponica_ cover

dila_h: _Diapensia lapponica_ height

emni_c: _Empetrum nigrum_ cover

emni_h: _Empetrum nigrum_ height

hahy_c: _Harimanella hypoides_ cover

hahy_h: _Harimanella hypoides_ height

lopr_c: _Loiseleuria procumbens_ cover

lopr_h: _Loiseleuria procumbens_ height

oxpa_c: _Oxycoccus palustre_ cover

oxpa_h: _Oxycoccus palustre_ height

phca_c: _Phyllodoce caerulea_ cover

phca_height: _Phyllodoce caerulea_ height

rhod_c: _Rhododendron_ sp. cover

rhod_h: _Rhododendron_ sp. height

saar_c: _Salix arctica_ cover

saar_h: _Salix arctica_ height

sagl_c: _Salix glauca_ cover

sagl_h: _Salix glauca_ height

sahe_c: _Salix herbacea_ cover

sahe_h: _Salix herbacea_ height

vaul_c: _Vaccinium uliginosum_ cover

vaul_h: _Vaccinium uliginosum_ height

drin_c: _Dryas integrifolia_ cover

drin_h: _Dryas integrifolia_ height

 Community characteristics

rich_pa: shrub species richness at grid level

rich: shrub species richness averaged across 3 1x1 m sampling quadrats per grid

shan: Shannon diversity (‘vegan’ package; Oksanen et al. 2019)

comp_bena: shrub competition on _Betula nana_ (i.e. summed cover of non-_B. nana_ species) [% cover]

comp_sagl: shrub competition on _Salix glauca_ (i.e. summed cover of non-_S. glauca_ species) [% cover]

ht_cwm: maximum shrub canopy height (i.e. community weighted mean by abundance of maximum shrub height) [mm]

 Topography and terrain wetness (calculated from)

tcws: Tasseled Cap Wetness component (Sentinal images)

slope: slope angle (MEaSUREs Greenland Ice Mapping Project Digital Elevation Model v. 1; Howat et al., 2014, 2015) [º]

twi: SAGA wetness index (MEaSUREs Greenland Ice Mapping Project Digital Elevation Model v. 1; Howat et al., 2014, 2015)

asp: aspect (MEaSUREs Greenland Ice Mapping Project Digital Elevation Model v. 1; Howat et al., 2014, 2015) [º]

 Downscaled climate (time series 1984 – 2013)

insoljja: average June-August insolation [MJ cm-2 yr-1]

precipmam: cumulative March-May precipitation [mm]

tempcont: yearly maximum – minimum temperature [ºC]

tempmin: yearly minimum temperature [ºC]

precipjja: cumulative June-August precipitation [mm]

tempjja: average maximum June-August temperature [ºC]

tempmax: yearly maximum temperature [ºC]

en: Nuup Kangerlua

en:
 Collected July-August 2011-2013 (PI: Jacob Nabe-Nielsen)

These data collected July-August 2011-2013 (PI: Jacob Nabe-Nielsen). Please contact J. Nabe-Nielsen (jnn_at_ecos.au.dk) to request access to data on all surveyed shrub species. Available here are only data used in Chardon et al. 2022.

 COLUMN ABBREVIATIONS

 Metadata for 90 m spatial grid

year: sampling year

alt: average altitude of grid as recorded during field surveys [m]

long: WGS84 longitude

lat: WGS84 latitude

x_stere: longitude in Polar Stereographic (EPSG 4326)

y_stere: latitude in Polar Stereographic (EPSG 4326)

 Species presence [1] or absence [0] at grid level

pa_bena: _Betula nana_

pa_sagl: _Salix glauca_

 Shrub species cover (calculated from pin hits in 0.7 x 0.7 m frame, based on total of 25 hits) [%]

cov_bena: _Betula nana_ cover

cov_sagl: _Salix glauca_ cover

 Downscaled climate (time series 1984 – 2013)

tempjja: average maximum June-August temperature [ºC]

tempmax: yearly maximum temperature [ºC]

tempmin: yearly minimum temperature [ºC]

tempcont: yearly maximum – minimum temperature [ºC]

precipmam: cumulative March-May precipitation [mm]

precipjja: cumulative June-August precipitation [mm]

insoljja: average June-August insolation [MJ cm-2 yr-1]

 Topography and terrain wetness (calculated from)

twi: SAGA wetness index (MEaSUREs Greenland Ice Mapping Project Digital Elevation Model v. 1; Howat et al., 2014, 2015)

slope: slope angle (MEaSUREs Greenland Ice Mapping Project Digital Elevation Model v. 1; Howat et al., 2014, 2015) [º]

asp: aspect (MEaSUREs Greenland Ice Mapping Project Digital Elevation Model v. 1; Howat et al., 2014, 2015) [º]

tcws: Tasseled Cap Wetness component (Sentinal images)

 Community characteristics

rich: shrub species richness averaged across pin-point frames per grid

shan: Shannon diversity (‘vegan’ package; Oksanen et al. 2019)

comp_bena: shrub competition on Betula nana (i.e. summed cover of non-_B. nana_ species) [% cover]

comp_sagl: shrub competition on Salix glauca (i.e. summed cover of non-_S. glauca_ species) [% cover]

en: GitLab Repository

en: Zip drive of GitLab repository contents (https://gitlab.com/nathaliechardon/gl_microclim).

en:
 Study Aim

We collected these data to alternatively train and validate high resolution (~ 90 m) Species Distribution Models (SDMs) and Species Abundance Models (SAMs) for _Betula nana_ L. (dwarf birch, Betulaceae) and _Salix glauca_ L. (grey willow, Salicaceae) in Southwest Greenland to assess how well such models can predict local-scale patterns.

 Data Description

Individual (presence-absence, abundance, maximum vegetative height) and community (species composition, maximum canopy height) shrub data for two fjords near Nuuk, Southwest Greenland. Also provided are corresponding downscaled climate data as well as calculated topographic and terrain wetness indicator variables.

 Nuup Kangerlua (Godthåbsfjord)

_Betula nana_ and _Salix glauca_ presence-absence, abundance, community species richness

 Kangerluarsunnguaq (Kobbefjord)

Shrub presence-absence, abundance, maximum vegetative height, community composition, maximum shrub canopy height

 Methods

 Field survey in Nuup Kangerlua

We conducted a stratified systematic plant survey along the length of Nuup Kangerlua (NK) fjord in Soutwesth Greenland (Fig. 1 in Chardon et al. 2022; following Nabe-Nielsen et al., 2017). At five distinct sites, we sampled along elevational gradients to collect data on presences, absences, abundance, and species composition of all woody species using a 0.7 x 0.7 m pin-point frame (Fig. 1e in Chardon et al. 2022). For model training, we converted these pin-point data to percent cover estimates based on the number of pins dropped (n = 25 per plot) and averaged them across the 119 spatio-climatic grids (see next section) corresponding to the plot locations (for details see Appendix S2 in Chardon et al. 2022).

 Field survey in Kangerluarsunnguaq

We conducted a random stratified plant survey in Kangerluarsunnguaq (K) fjord in Southwest Greenland. We used a preliminary Species Abundance Model trained with summed pin counts of _Betula nana_ in NK fjord (see Fig. S1.3 in Chardon et al. 2022) to stratify the ~ 27 x 17 km fjord landscape into low, medium, and high abundances classes. We randomly selected 90 x 90 m spatio-climatic grids to survey in each class for a total of 200 grids, ensuring that they were accessible by foot or boat (for details see Appendix S2 in Chardon et al. 2022). Within each grid, we sampled within three 1 m2 quadrats arranged in a randomly rotated equilateral triangle centered on the mid-point of the cell. We used a gridded sampling quadrat with 1% delineations (Fig. 1h in Chardon et al. 2022) to record woody species presences, absences, and composition, estimated percent cover, and measured maximum shrub species vegetatitve height. At every plot, we also visually scanned the area in a 20 m radius from the plot and recorded the presence of any additional shrub species to estimate grid-level species richness. As in NK fjord, we averaged these data at the grid level (for details see Appendix S2 in Chardon et al. 2022).

 Biotic variables

We calculated biotic microscale variables from the plant survey data collected in NK and K fjords. We calculated shrub species richness, diversity, and competition (i.e. sum of non-B. nana or non-S. glauca pin hits or percent cover). In K fjord, we also calculated canopy height as the community weighted mean (by abundance) of maximum vegetative shrub height.

 Climate variables

We computed high resolution temperature, precipitation, and insolation for local scale data for the study area by statistically downscaling climate time series (1982 - 2013) from the monthly CHELSA data (Karger et al. 2017). We downscaled these data from 30 arc sec (~ 400 m at the latitude of our study) to our target grid size of ~ 90 m with geographic weighted regression and using the MEaSUREs Greenland Ice Mapping Project (GIMP) Digital Elevation Model (DEM) v. 1 (Howat et al., 2014, 2015). We then calculated 30-year averages of the climate parameters: average summer (June – August) maximum temperature, yearly maximum temperature, yearly minimum temperature, temperature continentality (yearly max. - min. temperatures), cumulative Spring (March – May) precipitation, cumulative summer precipitation, and average summer incident solar radiation (henceforth, insolation) (for calculation details see Appendices S2, S3 in Chardon et al. 2022 and Appendix S2 in von Oppen et al. 2021).

 Topography and terrain wetness indicator variables

We calculated several topographic and terrain wetness indices at a local scale. We derived slope, aspect, and the SAGA wetness index (hereafter TWI; Boehner et al., 2002; Boehner and Selige, 2006) from the GIMP DEM. TWI is a measure of how ‘wet’ an area is, based on water drainage from the surrounding landscape. We also calculated the tasseled cap wetness component (hereafter TCW, Crist and Cicone 1984) from satellite images (for details see Appendices S2, S3 in Chardon et al. 2022) as an alternative measure of wetness.

 Computer code

Attached as zip file and available on GitLab (https://gitlab.com/nathaliechardon/gl_microclim)

 Third-party data

Data used to calculate climate, topography, and terrain wetness indicator variables are publicly available (see Appendix S2 in Chardon et al. 2022 for all data references).

accessible-shrub-forest

display_name: accessible-shrub-forest

arctic

display_name: arctic

climate

display_name: climate

field-data

display_name: field-data

sdm

display_name: sdm

validation

display_name: validation

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: Greenland shrubs and microclimate


en: biodiversity microclimate forest climate-change statistical-interpolation radiation-transfer ecology

en: Predicted microclimate air temperatures at 100 cm above ground. 10 m spatial resolution raster files are provided for mean daily minimum (tmin), mean (tmean) and maximum (tmax) temperatures during each month from April (04) to October (10) over the period between 2012 to 2021.

en: Predicted microclimate topsoil temperatures at 5 cm below ground. 10 m spatial resolution raster files are provided for mean daily minimum (tmin), mean (tmean) and maximum (tmax) temperatures during each month from April (04) to October (10) over the period between 2012 to 2021.

en: Predicted microclimate air temperatures at 5 cm above ground. 10 m spatial resolution raster files are provided for mean daily minimum (tmin), mean (tmean) and maximum (tmax) temperatures during each month from April (04) to October (10) over the period between 2012 to 2021.

en: Climate data matching the scales at which organisms experience climatic conditions are often missing. Yet, such data on microclimatic conditions are required to better understand climate-change impacts on biodiversity and ecosystem functioning. Here we combine a national network of microclimate temperature measurements with a novel radiative transfer model to map monthly minimum, mean and maximum temperatures during the vegetation period at a 10 meter spatial resolution across Switzerland. The temperature measurements took place in 107 sampling plots distributed across different habitat types, with 62 plots in forests, 22 below trees outside forests, and 23 in open grasslands. In each plot we measured temperature in the topsoil (-5cm), as well as in the air at 5cm and 100cm height above ground. Spatial interpolation was achieved by using a hybrid approach based on linear mixed effects models with input from detailed radiation estimates that account for topographic and vegetation shading, as well as other predictor variables related to the macroclimate, topography and vegetation height. Our data reveals strong horizontal and vertical variability in microclimate temperature, particularly for maximum temperatures at 5 cm above the ground and within the topsoil. Compared to macroclimate conditions as measured by weather stations outside forests, diurnal air and topsoil temperature ranges inside forests were reduced by up to 3.0 and 7.8 °C, respectively, while below trees outside forests, e.g. in hedges and below solitary trees, this buffering effect was 1.8 and 7.2 °C. We also found that in open grasslands, maximum temperatures at 5 cm above ground are on average 3.4 °C warmer than that of macroclimate, suggesting that in such habitats heat exposure close to the ground is often underestimated when using macroclimatic data. After accounting for macroclimate effects, microclimate patterns were primarily driven by radiation, with particularly strong effects on maximum temperatures. Results from spatial block cross-validation revealed predictive accuracies as measured by RSME’s ranging from 1.18 to 3.43 °C, with minimum temperatures generally being predicted more accurately than maximum temperatures. The microclimate maps presented here enable a more biologically relevant perspective when analysing climate-species interactions, which is expected to lead to a better understanding of biotic and ecosystem responses to climate and land use change.

biodiversity

display_name: biodiversity

climate-change

display_name: climate-change

ecology

display_name: ecology

forest

display_name: forest

microclimate

display_name: microclimate

radiation-transfer

display_name: radiation-transfer

statistical-interpolation

display_name: statistical-interpolation

en: Monthly topsoil and near surface microclimate temperature data for Switzerland


greenland-climate-network-gc-net-data

title_for_slug: greenland-climate-network-gc-net-data

en: greenland aws air-temperature automatic-weather-station net-radiation climate

en: 22-Petermann ELA

en: GC Net Chart Parameters

media_type: application/json

en: Stations parameters from static bucket

format: JSON

en: Access the latest L1 data

en:
The GC-Net is kindly continued by the Geological Survey of Denmark and Greenland (GEUS).

Starting October 3, 2022, the access to the latest versions of the "ready to use" L1 data has been migrated to GEUS, (doi:10.22008/FK2/VVXGUT). Future versions will be available from GEUS, while the initial version of L1 data has been archived.

en: Archived GC-Net Data (deprecated)

en:
The GC-Net is kindly continued by the Geological Survey of Denmark and Greenland (GEUS).

Starting October 3, 2022, the access to the latest versions of the "ready to use" L1 data has been migrated to GEUS, (doi:10.22008/FK2/VVXGUT). Future versions will be available from GEUS, while the initial versions of L0 and L1 data have been archived.

en: GC Net Config for Stations

en: Stations Config from the static bucket

en:
In Memory of Dr. Konrad (Koni) Steffen

Update October 2022: The GC-Net is kindly continued by the Geological Survey of Denmark and Greenland (GEUS).
Starting October 3, 2022, the access to the latest versions of the "ready to use" L1 data has been migrated to GEUS. Future data versions will be available at: [https://doi.org/10.22008/FK2/VVXGUT](https://doi.org/10.22008/FK2/VVXGUT)
 Background
Starting with a single station in 1991, the Greenland Climate Network (commonly known as GC-Net) is a set of Automatic Weather Stations (AWS) set up and managed by the late Prof. Dr. Konrad (Koni) Steffen, and spanning the Greenland Ice Sheet (GrIS). This first station was "Swiss Camp" or the "ETH-CU" camp (GC-Net station 01) which was used as a field science and education site by Koni for years. The GC-Net was expanded with multiple NASA, NOAA, and NSF grants throughout the years, and then supported by WSL in the later years. These data (see "C-file" below) were previously hosted by the Cooperative Institute for Research in Environmental Sciences (CIRES) in Boulder, Colorado.

 Overview
Provided in this dataset are the 16 longest running stations in the network, which are spread over a significant area of the GrIS and the majority of the unique climatic zones. From the South Dome high point in the South, to the Western Jakobshavn ablation region in the west, to the Petermann glacier in the North across east of the Northeast Greenland Ice Stream to the east, GC-Net is the longest running climatological record of Greenland.

 The standard GC-Net station consists of:
* Air temperature measurements at 2 heights above the surface
* Temperature and humidity measurements at 2 heights above the surface
* Wind speed and direction measured at 2 heights above the surface
* Sonic distance sounder measurements for 2 snow height and distance of instruments to surface
* Incoming shortwave radiation measurement
* Reflected shortwave radiation measurement
* Net broadband radiation (long- and short-wave) measurement
* Air pressure measurement
Data have often been repatriated in near-real time using one of either the GOES geostationary satellite or the ARGOS polar orbiting satellite transmission system. The stations were visited typically every 1-2 years for maintenance and service, and to download full uncorrupted data directly from the dataloggers. GC-Net stations were visited by Twin Otter equipped with snow skids to land directly on the open-ice at the AWS locations, or by helicopter near the west coast. The AWSs operate on solar and battery power and occasionally lost power during the dark and cold winter months, particularly when the batteries were aging.

 Dataset
This dataset consists of 2 main data levels; Level 0 and Level 1.
Level 0 is the raw data from the dataloggers, historical processing codes, satellite transmissions, and Koni’s personal data archive. Level 0 data (.zip) directories contain subdirectories:
* “C file” - contains the historical processed datafile for each station.
* “Campbell logger files” - contains the raw csv datafiles from the stations’ Campbell Scientific dataloggers since the CR1000 era (~2007-2008 for most stations).
* “Photos” - contains photographs of the station when available marked by year.
Level 1 is the appended, calibrated, cleaned, and quality flagged data. The full processing scheme is open-source and publicly available on the following GitHub repository (please also check GitHub for the latest L1 data):
[GC-Net L1 data on GitHub](https://github.com/GEUS-Glaciology-and-Climate/GC-Net-level-1-data-processing "GC-Net-level-1-data-processing")
Level 1 data is provided in the newly described csv-compatible [NEAD format](https://www.envidat.ch/#/metadata/nead "NEAD format").

 Additional Details
Dataset description publication will be forthcoming.
The Geological Survey of Denmark and Greenland (GEUS) has been imperative in the reprocessing and continuity mission of GC-Net. Multiple GC-Net stations have been replaced with updated and upgraded AWS hardware at the same coordinates by GEUS. This effort will ensure continuity of the GC-Net dataset into the future.

air-temperature

display_name: air-temperature

automatic-weather-station

display_name: automatic-weather-station

aws

display_name: aws

greenland

display_name: greenland

net-radiation

display_name: net-radiation

en: Greenland Climate Network (GC-Net) Data


swiss-fluxnet-site-lageren

title_for_slug: swiss-fluxnet-site-lageren

en: greenhouse-gas swiss-forest-lab eddy-covariance meteorological-measurements forest swiss-fluxnet flux

en: Data access

media_type: text/html

en: The flux and meteo data of the Swiss FluxNet site Lägeren are openly available from the European Fluxes Database Cluster.

format: HTML

en: Site description

en:
The Swiss FluxNet Site Lägeren is a managed mixed deciduous mountain forest located on the steep Lägeren mountain (NW of Zurich, Swiss Plateau). The forest is highly diverse, dominated by beech, but also including ash, maple, spruce and fir trees. Eddy covariance flux measurements were started in April 2004. The site was part of the international CarboEurope IP network and the National Air Pollution Monitoring Network (NABEL). In addition to Swiss FluxNet, the site is part of the Long-term Forest Ecosystem Research (LWF) of WSL and the biological drought and growth indicator network (TreeNet) of WSL.

Measurements

- Ecosystem flux measurements of CO2, H2O vapour are performed with the eddy-covariance method. This method is based on measurements of trace gas mixing ratios, using infrared gas analyzers (for CO2, H2O vapor), combined with wind speed and wind direction measurements, using 3D sonic anemometers. To resolve the short-term turbulent fluctuations in the atmosphere, very fast measurements are needed: we measure at 10-20 Hz, i.e., 10-20 times per second. To assess the energy budget of each ecosystem, also radiation sensors and soil climate profiles are installed at the site.
- Sub-canopy eddy fluxes (CO2, H2O), soil respiration campaigns
- Continuous CO2 profile measurements.
- Auxiliary micrometeorology and soil climate measurements.

Data availability

All data are available from the European Fluxes Database Cluster, but are also part of Fluxnet2015 dataset.

Data policy

ICOS data license:
[https://www.icos-cp.eu/data-services/about-data-portal/data-license](https://www.icos-cp.eu/data-services/about-data-portal/data-license)

Detailed site info:
[https://www.swissfluxnet.ethz.ch/index.php/sites/ch-lae-laegeren/site-info-ch-lae//](https://www.swissfluxnet.ethz.ch/index.php/sites/ch-lae-laegeren/site-info-ch-lae/)

eddy-covariance

display_name: eddy-covariance

flux

display_name: flux

greenhouse-gas

display_name: greenhouse-gas

meteorological-measurements

display_name: meteorological-measurements

swiss-fluxnet

display_name: swiss-fluxnet

swiss-forest-lab

display_name: swiss-forest-lab

educ

en: Education, culture and sport

envidat

en: EnviDat: the Environmental Data Portal

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

en: Swiss FluxNet Site Lägeren


en: meteorological-data climate-change europe climate climate-indicators forest-fire mountains indicator-values fire european-alps

en: This dataset contains the Fire Weather Index for Hydrological Bavaria from 1980 - 2099 as stated in the paper "Climate change impacts on regional fire weather in heterogeneous landscapes of Central Europe" published in Natural Hazards and Earth System Sciens (NHESS) 2023. The dataset contains daily Fire Weather Index values for all 50 members (subfolders of the dataset) of the CRCM5-LE (11 km spatial resolution) from 1980 to 2099 over the domain of Hydrological Bavaria. Please cite this dataset as the publication: Miller, J., Böhnisch, A., Ludwig, R., & Brunner, M. I. (2023). Climate change impacts on regional fire weather in heterogeneous landscapes of Central Europe. Natural Hazards and Earth System Sciences Discussions, 1-25. doi: 10.5194/nhess-2023-51.

climate

display_name: climate

climate-change

display_name: climate-change

climate-indicators

display_name: climate-indicators

europe

display_name: europe

european-alps

display_name: european-alps

fire

display_name: fire

forest-fire

display_name: forest-fire

indicator-values

display_name: indicator-values

meteorological-data

display_name: meteorological-data

mountains

display_name: mountains

en: Fire Weather Index for Hydrological Bavaria from 1980-2099 derived from the 50 member CRCM5-LE


maintainer: Leo Gallus Bont

en: swisstopo qgis-plugin digital-planning seilaplan swiss-geodata open-source geoinformation-software digital-elevation-model cable-yarding

en: Herunterladen des DHM von swisstopo Website

en: View video on youtube!

en:
In order to use the QGIS plugin ‘Seilaplan’ for digital cable line planning, a digital terrain model (DTM) is required. As an alternative to using the ‘Swiss Geo Downloader’ plugin, the DTM can be obtained directly from Swisstopo. In this tutorial we explain step by step how to download the necessary DTM from the Swisstopo Website, and how to use it in QGIS for the digital planning of a cable line using the plugin ‘Seilaplan’. Please note that the tutorial language is German!

Link to the elevation model on the swisstopo website: https://www.swisstopo.admin.ch/de/geodata/height/alti3d.html#technische_details

Link to the rope map website: https://seilaplan.wsl.ch

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

Für die Verwendung des QGIS Plugins Seilaplan zur digitalen Seillinienplanung ist ein digitales Höhenmodell (DHM) nötig. Als Alternative zum Swiss Geo Downloader erklären wir in diesem Tutorial Schritt für Schritt, wie man das nötige Höhenmodell von der Swisstopo Webseite herunterladen und in QGIS zur Seillinienplanung verwenden kann.

Link zum Höhenmodell auf der swisstopo Webseite: https://www.swisstopo.admin.ch/de/geodata/height/alti3d.html#technische_details

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

cable-yarding

display_name: cable-yarding

digital-elevation-model

display_name: digital-elevation-model

digital-planning

display_name: digital-planning

geoinformation-software

display_name: geoinformation-software

open-source

display_name: open-source

qgis-plugin

display_name: qgis-plugin

seilaplan

display_name: seilaplan

swiss-geodata

display_name: swiss-geodata

swisstopo

display_name: swisstopo

en: Seilaplan Tutorial: DTM download from swisstopo website


en: avalanche snowpack source-code snow-modelling snowdrift

en:
This dataset includes the FORTRAN code of the FSM2trans model version used in the paper: Quéno et al., Snow redistribution in an intermediate-complexity snow hydrology modelling framework, The Cryosphere, 2024.
The FSM2trans code is derived from the FSM2 model (Essery et al., 2015) and its variant FSM2oshd (Mott et al., 2023). In this model, we implemented and adapted the snowdrift model SnowTran-3D (Liston et al., 2007) and the avalanching model SnowSlide (Bernhardt and Schulz, 2010).
This dataset does not include the processing scripts to prepare meteorological input data for the model, provided as bin files.

avalanche

display_name: avalanche

snow-modelling

display_name: snow-modelling

snowdrift

display_name: snowdrift

snowpack

display_name: snowpack

source-code

display_name: source-code

en: FSM2trans code