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zenodo40/100

Unexpected microbial metabolic responses to elevated temperatures and nitrogen addition in subarctic soils under different land-use

<p>This repository contains all necessary raw data as well as the R code used to conduct statistical analysis and create figures of the publication<br>&nbsp;<br><strong>Unexpected microbial metabolic responses to elevated temperatures and nitrogen addition in subarctic soils under different land-use</strong></p><p>Julia Schroeder1, Tino Peplau1, Edward Gregorich2, Christoph C. Tebbe3, Christopher Poeplau1</p><p>1 Thünen Institute of Climate-Smart Agriculture, Bundesallee 68, 38116 Braunschweig, Germany<br>2 Research and Development Centre, Central Experimental Farm, Agriculture and Agri-Food Canada, Ottawa, Canada<br>3 Thünen Institute of Biodiversity, Bundesallee 65, 38116 Braunschweig, Germany</p><p>DOI: https://doi.org/10.1007/s10533-022-00943-7&nbsp;</p><p>This study investigated how subarctic soils under different land use will respond to warming and increasing N availability to allow for better predictions of C cycling under global change. The short-term temperature sensitivity as well as N-input effects on microbial CUE, respiration, growth and turnover were assessed in a one-day incubation experiment according to the 18O-CUE approach. The warming and N response of SOM decomposition were assessed in a 50-days incubation experiment via measurement of cumulative respiration. Both experiments were conducted with the following three treatments: incubation at 10 °C, incubation at 20 °C, and incubation at 20 °C plus N-fertiliser addition at an amendment rate of 100 kg N ha-1. The response to warming or N addition were expressed as response ratios RRT = 20°C/10°C and RRN = 20°C+N/20°C for warming and N response, respectively.</p><p>The R code was developed under R v3.6.3 and adapted to work under version R v.4.1.2.</p><p>The repository includes the following files:</p><ul><li>general_soil_parameters_per_sample.csv - general soil data for each field sample (n=27)</li><li>general_soil_parameters_per_plot.csv - general soil data assessed on pooled replicated field samples (n=9)</li><li>respiration_over_50d_incubation.csv - respiration rate and cumulative respiration for each time-point and laboratory sample over the 50-days incubation</li><li>sample_data.csv - data measured for each laboratory sample (n=81)</li></ul><p>&nbsp;</p><ul><li>Warming_and_nitrogen_response_of_CUE_in_subarctic_soils.Rproj - Rproject (load project to work on provided scripts and data)</li><li>load_data_script.R - loads required data</li><li>absolute_values_script.R - summary of absolute ranges of parameters per land-use type and site</li><li>absolute_linear_mixed_effects_model_script.R - run statistical analysis</li><li>correlograms_absolute_soil_params_script.R - correlation analysis to identify what drives absolute values</li><li>plot_correlations_absolute_soil_params_script.R - plot drivers of CUE and cumulative respiration</li><li>RRT_RRN_calculation_script.R - calculates response ratios</li><li>plot_RRT_RRN_script.R - plot response ratios</li><li>RRT_RRN_linear_mixed_effects_models_script.R - run statistical analysis</li><li>correlograms_RRT_RRN_soil_param_script.R - correlation analysis to identify drivers of response ratios</li><li>plot_correlations_RRT_RRN_soil_params_script.R - plot drivers of response ratios</li><li>RRT_RRN_resprate_cumulresp_over_time_50d_incubation_script.R - plot response ratios over time course</li></ul>

opencc-by-4.0Apr 2022View details →
zenodo40/100

Number of chamber measurement locations for accurate quantification of landscape-scale greenhouse gas fluxes: Importance of land use, seasonality, and greenhouse gas type

<p>Contains all raw data measured in the Schwingbach Earth Observatory (SEO) from Spring, Summer and Autumn 2020. Data was measured with an on-site LGR laser from the GHG emissions, and with 100cm&sup3; soil cores for the soil characteristics. Details can be found in the corresponding manuscript &quot;Number of chamber measurement locations for accurate quantification of landscape-scale greenhouse gas fluxes: Importance of land use, seasonality, and greenhouse gas type&quot;</p>

opencc-by-4.0Jul 2022View details →
zenodo40/100

A Google Earth Engine code to analyze e visualize land surface temperature and thermal hot-spot patterns: a Rome (Italy) case study

<p>Link to the&nbsp;<strong>Google Earth Engine </strong>(GEE) code: <strong>https://code.earthengine.google.com/cc3ea6593574e321acd7b68c975a9608</strong></p> <p>You can&nbsp;analyze and visualize the following spatial layers by accessing the&nbsp;GEE link:&nbsp;</p> <ol> <li><strong>Daytime summer land surface temperature</strong>&nbsp;(raster data, 30 m horizontal&nbsp;resolution, from Landsat-8 remote sensing data, years 2017-2022)</li> <li><strong>The surface thermal hot-spot pattern&nbsp;</strong>(raster data,30 m&nbsp;horizontal&nbsp;resolution) was&nbsp;obtained by using a statistical-spatial method based on the Getis-Ord Gi* approach through the ArcGIS&nbsp;tool.&nbsp;</li> </ol> <p>Here attached the .txt&nbsp;file from&nbsp;the&nbsp;<strong>GEE code</strong>.&nbsp;</p> <p>&nbsp;</p> <p><em>E-mail</em></p> <p>Giulia Guerri, CNR-IBE, giulia.guerri@ibe.cnr.it</p> <p>Marco Morabito, CNR-IBE, marco.morabito@cnr.it</p> <p>Alfonso Crisci, CNR-IBE, alfonso.crisci@ibe.cnr.it</p>

opencc-by-4.0Jul 2022View details →
zenodo40/100

General causal loop diagram of main land-sea interactions for the Belgian coastal zone.

<p>This is a polished&nbsp;diagram of the main causal land-sea interactions, based on aggregation of the detailed mind maps of land-sea interactions identified by the coastal and rural stakeholders who participated in the Belgian Multi-Actor Lab of the EU-funded H2020 project COASTAL (https://h2020-coastal.eu). The diagrams are used for designing System Dynamics models and evidence-based business road maps.&nbsp;&nbsp;</p>

opencc-by-4.0Nov 2021View details →
zenodo40/100

Generating Annual 4-m Land Cover Products over 28 Metropolises in China during 2000-2020

<p>A 4-m fine-grained land cover products over the 28 provincial capital cities in China (mainly in temperate&nbsp;monsoon climate and subtropical monsoon climate zone, and categorized into 7 classes, i.e.,&nbsp;cropland, forest, grass, shrub, water, impervious surface, and bare land) is generated through&nbsp;the proposed model; A 4-m annual land cover products during 2000-2020 in Wuhan, China&nbsp;is generated through the proposed model.</p> <p>To validate the effectiveness of the derived products, three verification approaches are employed. 1) evaluation by the consistency with the contemporary products including 10-m Esri Land Cover,&nbsp;10-m FROMGLC10, and 30-m GlobeLand30 ; 2) evaluation by the publicly certified 4-m&nbsp;annotation dataset GID; 3) evaluation by the third-party-created annotation samples. The&nbsp;validation results can be viewed in the manuscript, and the reproduction executation details can be viewed at Readme.txt.</p> <p>The products is in .tif format, and validaiton region&nbsp;is in ENVI/hdr format. Users need to&nbsp;install ENVI software or Arcgis to read the product.</p> <p>&quot;open_source_DETNet_code_and_simple_demo.rar&quot; is open source code and the corresponding intruction.</p>

opencc-by-4.0Jan 2022View details →
zenodo40/100

Fig. 5. A in Shell Morphology, Growth Pattern And Population Dynamics Of The Land Snail Xerolenta Obvia (Menke, 1828) In Two Areas Of Different Climatic Conditions Within A Temperate Climate Region

Fig. 5. A) Mean monthly whorl increment of Xerolenta obvia in two growth seasons in SW (solid line) and NE (dashed line) populations; B) mean (black lines), maxi- mum and minimum (grey lines) monthly temperature, and C) total monthly precipitation during the study period in SW (solid lines) and NE (dashed lines) sites. Data from nearest meteorological stations in Wrocław and Suwałki (IMGW-PIB data)

opencc-by-4.0Mar 2020View details →
zenodo40/100

Fig. 2 in Shell Morphology, Growth Pattern And Population Dynamics Of The Land Snail Xerolenta Obvia (Menke, 1828) In Two Areas Of Different Climatic Conditions Within A Temperate Climate Region

Fig. 2. Distribution of shell pattern types of Xero- lenta obvia snails in the two populations studied, SW (n = 781) and NE (n = 1387)

opencc-by-4.0Mar 2020View details →
zenodo40/100

Interactions between land use, taxonomic group and aspects and levels of diversity in a Brazilian savanna: implications for the use of bioindicators

<p>The study was carried out&nbsp;in&nbsp;the&nbsp;Tri&acirc;ngulo&nbsp;Mineiro region of Minas Gerais state, covering the municipalities of&nbsp;Uberl&acirc;ndia, Monte&nbsp;Alegre,&nbsp;and Nova Ponte,&nbsp;in&nbsp;south-eastern&nbsp;Brazil.&nbsp;We&nbsp;conducted the study&nbsp;in&nbsp;five habitat types,&nbsp;comprising&nbsp;two&nbsp;natural&nbsp;habitats&nbsp;(savanna&nbsp;and&nbsp;semideciduous forest),&nbsp;and three anthropogenic land-uses:&nbsp;cattle pastures (planted with&nbsp;introduced&nbsp;Urochloa&nbsp;grasses),&nbsp;soy fields (where sampling took place when plants were at the vegetative phase)&nbsp;and&nbsp;&nbsp;plantations&nbsp;of&nbsp;Eucalyptus&nbsp;trees&nbsp;(&ge;&nbsp;6&nbsp;yrs&nbsp;old).&nbsp;Ants&nbsp;and beetles&nbsp;were sampled&nbsp;at&nbsp;the same&nbsp;40 sites (8&nbsp;replicates&nbsp;per&nbsp;land use), and birds&nbsp;at&nbsp;30 sites (6&nbsp;replicates&nbsp;per land use), only some of which were the same as for ants and beetles.&nbsp;</p> <p>Ants&nbsp;that forage on ground&nbsp;and&nbsp;dung beetles&nbsp;were sampled&nbsp;using&nbsp;pitfall traps. Sampling took&nbsp;place in&nbsp;November&nbsp;and December&nbsp;(early wet season)&nbsp;2017.&nbsp;In each site, eight traps were&nbsp;installed with traps located at the corners of a 100&times;100&nbsp;m square, and at the mid-points of&nbsp;the sides of the square,&nbsp;keeping a&nbsp;minimum distance of 50&nbsp;m between&nbsp;any two&nbsp;traps.&nbsp;All traps were at least 75 m distant from the edge of the respective land&nbsp;use.&nbsp;Traps were plastic containers (19 cm&nbsp;diam, 11 cm height) filled with 150 ml of a saline solution and detergent. Each trap had a wire hoop suspended over it to accommodate a small (4 cm&nbsp;diam, 4 cm height) plastic container for holding a dung bait. We used a 20 cm&nbsp;diameter plastic cover supported by three sticks to protect traps from rain. Traps were baited with&nbsp;~40 g of a mixture of pig dung and human&nbsp;faeces&nbsp;(4:1 proportion)&nbsp;and left in the field for 48-hrs.</p> <p>Birds were surveyed&nbsp;using&nbsp;20-min point counts in the rainy season (November 2017 to March 2018). At each site,&nbsp;five sampling points were established, 200 m distant from each other. All surveys started at sunrise (about 6 a.m.), and all species seen or heard from each point were recorded. Each sampling site was&nbsp;re-surveyed&nbsp;in the&nbsp;following&nbsp;dry season (April to&nbsp;October to 2018); however, for logistic reasons we were unable to re-survey the plantation sites.&nbsp;</p> <p>Ant&nbsp;and dung beetle&nbsp;species were identified to&nbsp;species or morphospecies&nbsp;by comparison with named species in the Zoological Collection at the Federal University of&nbsp;Uberl&acirc;ndia&nbsp;(UFU)&nbsp;or&nbsp;with&nbsp;specialist assistance from Fernando Vaz de Mello, respectively.&nbsp;Vouchers of&nbsp;all&nbsp;species have been deposited&nbsp;at&nbsp;UFU&acute;s Zoological Collection.&nbsp;Birds were identified directly in the field and species&nbsp;names follow the checklist produced by the Brazilian Ornithological Records Committee.</p> <p>We classified species&nbsp;functionally&nbsp;based on&nbsp;primary diet, foraging&nbsp;location&nbsp;and/or&nbsp;behaviour, and body size,&nbsp;as&nbsp;these&nbsp;traits&nbsp;are known to be sensitive&nbsp;to habitat modifications&nbsp;and of importance for the ecosystem services provided by ants, birds, and dung beetles.</p> <p>Ant species were classified according to their diet as&nbsp;predators,&nbsp;fungivores,&nbsp;nectarivores&nbsp;or omnivores,&nbsp;and according to their main foraging location&nbsp;as arboreal, epigeal&nbsp;(aboveground)&nbsp;or hypogeal&nbsp;(in soil and litter), based on&nbsp;information provided by Brown (2000) and Silvestre&nbsp;et al.&nbsp;(2003). Species were&nbsp;further&nbsp;classified&nbsp;into four body size categories based on&nbsp;our&nbsp;measurements of body length&nbsp;(Weber&acute;s length;&nbsp;Brown,&nbsp;1953)&nbsp;of&nbsp;1-5&nbsp;ant workers&nbsp;per species:&nbsp;1 (&lt; 0.75&nbsp;mm),&nbsp;2 (0.75-1.74&nbsp;mm),&nbsp;3 (1.75-3&nbsp;mm),&nbsp;and 4 (&gt; 3 mm).</p> <p>Dung beetles were classified as coprophagous, necrophagous, frugivore, generalist or predator, according to the type of food resource each species is most&nbsp;often&nbsp;attracted to. This classification was based on over 30 years of field experience&nbsp;throughout Brazil&nbsp;by one of the authors&nbsp;of this study&nbsp;(FVM),&nbsp;who used multiple types of baits&nbsp;(e.g., carcasses, fruits, faeces)&nbsp;to attract and collect dung beetles, and/or on literature information.&nbsp;Although information about the &ldquo;attractiveness&rdquo; of different types of baits&nbsp;to&nbsp;dung beetles (used here as a proxy for primary diet)&nbsp;was&nbsp;not obtained&nbsp;directly&nbsp;in the sites of the present study, it is importat to note that we are not aware of&nbsp;any evidence&nbsp;of geographic or habitat&nbsp;variation in bait preference&nbsp;among tropical species of dung beetles.&nbsp;Dung beetles&nbsp;were also&nbsp;classified&nbsp;according&nbsp;to&nbsp;their&nbsp;foraging&nbsp;behaviour as:&nbsp;telecoprid&nbsp;(species that make a dung ball and roll it away for burial),&nbsp;paracoprid&nbsp;(species that store dung in tunnels dug immediately below the dung&nbsp;source),&nbsp;or&nbsp;endocoprid&nbsp;(species living within or immediately below the dung, without moving it).&nbsp;For this,&nbsp;we used&nbsp;the database of the&nbsp;Zoological Collection&nbsp;of&nbsp;the Federal University&nbsp;of&nbsp;Mato Grosso (UFMT).&nbsp;Whenever sample sizes&nbsp;allowed, 30&nbsp;individuals from each species&nbsp;were weighed for determination of body mass&nbsp;(following Almeida et al.,&nbsp;2011), and species were&nbsp;classified&nbsp;according to the following ordinal scale: 1&nbsp;(&lt;&nbsp;10&nbsp;mg);&nbsp;2&nbsp;(10-99&nbsp;mg);&nbsp;3&nbsp;(100-300&nbsp;mg);&nbsp;and&nbsp;4&nbsp;(&gt;300&nbsp;mg).</p> <p>Each bird&nbsp;species&nbsp;was&nbsp;classified according to&nbsp;its&nbsp;primary diet as&nbsp;frugivores granivore, insectivore, nectarivore,&nbsp;carnivore,&nbsp;detritivore,&nbsp;or omnivore,&nbsp;and according to the main&nbsp;foraging&nbsp;location&nbsp;as&nbsp;ground, understory/shrubby vegetation, or tree canopy, based on&nbsp;the&nbsp;Wilman&nbsp;et al.&nbsp;(2014) database and&nbsp;our&nbsp;own&nbsp;field experience.&nbsp;Using these&nbsp;same sources,&nbsp;we obtained information&nbsp;on&nbsp;mean body weights of each&nbsp;species and&nbsp;assigned&nbsp;them&nbsp;to one of&nbsp;five&nbsp;size categories: 1-&nbsp;(&lt;15 g);&nbsp;2&nbsp;(15-39 g);&nbsp;3&nbsp;(40-199&nbsp;g);&nbsp;4&nbsp;(200-599 g);&nbsp;and 5&nbsp;(&gt;&nbsp;600 g).</p>

opencc-by-4.0Aug 2022View details →
dryad40/100

Over the hills and through the farms: Land use and topography influence genetic connectivity of northern leopard frog (Rana pipiens) in the Prairie Pothole Region

<p><em>Context</em></p> <p>Agricultural land-use conversion has fragmented prairie wetland habitats in the Prairie Pothole Region (PPR), an area with one of the most wetland-dense regions in the world. This fragmentation can lead to negative consequences for wetland obligate organisms, heightening risk of local extinction and reducing evolutionary potential for populations to adapt to changing environments.</p> <p><em>Objectives</em></p> <p>This study models biotic connectivity of prairie-pothole wetlands using landscape genetic analyses of the northern leopard frog (<em>Rana pipiens</em>) to: (1) identify population structure and (2) determine landscape factors driving genetic differentiation and possibly leading to population fragmentation.</p> <p><em>Methods</em></p> <p>Frogs from 22 sites in the James River and Lake Oahe river basins in North Dakota were genotyped using Best-RAD sequencing at 2868 bi-allelic single nucleotide polymorphisms (SNPs). Population structure was assessed using STRUCTURE, DAPC, and fineSTRUCTURE. Circuitscape was used to model resistance values for ten landscape variables that could affect habitat connectivity.</p> <p><em>Results</em></p> <p>STRUCTURE results suggested a panmictic population, but other more sensitive clustering methods identified six spatially organized clusters. Circuit theory-based landscape resistance analysis suggested land use, including cultivated crop agriculture, and topography were the primary influences on genetic differentiation.</p> <p><em>Conclusions</em></p> <p>While the <em>R. pipiens</em> populations appear to have high gene flow, we found a difference in the patterns of connectivity between the eastern portion of our study area which was dominated by cultivated crop agriculture, versus the western portion where topographic roughness played a greater role. This information can help identify amphibian dispersal corridors and prioritize lands for conservation or restoration.</p>

opencc-zeroAug 2022View details →
zenodo40/100

Land use and land cover changes in the contiguous United States from 1630 to 2020

<p>Through integrating multi-source data including high-resolution remote sensing image-based land use and land cover (LULC) data, model-based land use products, and historical land archives, we reconstructed historical LULC at an annual time scale and 1 km x 1 km resolution in the contiguous United States (CONUS) from 1630 to 2020. Compared to other historical LULC datasets, our data can capture the major characters of LULC as well as provide more accurate information with higher spatial and temporal resolution. The LULC data can be used for regional studies in a wide range of topics including LULC impacts on the ecosystem, biodiversity, water resource, carbon and nitrogen cycles, and greenhouse gas emissions.</p>

opencc-by-4.0Mar 2022View details →
zenodo40/100

Data for: A spatial framework for prioritizing biochar application to arable land: a case study for Sweden

<p>The uploaded data is related to the publication:&nbsp;<em>A spatial framework for prioritizing biochar application to arable land: a case study for Sweden</em>, and&nbsp;contains the following:</p> <p>(I) Raster files for three different biochar prioritization narratives.</p> <p>(II) High-resolution biochar use indication maps (in JPEG) for different prioritization narratives.&nbsp;</p>

opencc-by-4.0Sep 2022View details →
zenodo40/100

Realizing COP26's declaration on deforestation protects forests at the expense of non-forest land

<p>Data and model source code for the manuscript: &quot;Realizing COP26&#39;s declaration on deforestation protects forests at the expense of non-forest land&quot;</p> <p>Abhijeet Mishra1,2,*, Florian Humpen&ouml;der1, Christopher P.O. Reyer1, Felicitas Beier1,2, Hermann Lotze-Campen1,2, and Alexander Popp1</p> <p>1 Potsdam Institute for Climate Impact Research (PIK), Member of Leibniz Association, P.O.Box 60 12 03, 14412,6<br> Potsdam, Germany<br> 2 Humboldt University of Berlin, Department of Agricultural Economics, Unter den Linden 6, 10099 Berlin,8<br> Germany</p> <p>Abhijeet Mishra<br> *mishra@pik-potsdam.de<br> September 2022</p> <p>See https://github.com/abhimishr/magpie/releases and https://github.com/magpiemodel/magpie/releases/tag/v4.5.0 for further details</p>

opencc-by-4.0Sep 2022View details →
dryad40/100

Data associated with: Emergence of the physiological effects of elevated CO2 on land-atmosphere exchange of carbon and water

<p>Elevated atmospheric CO<sub>2</sub> (eCO<sub>2</sub>) influences the carbon assimilation rate and stomatal conductance of plants and thereby can affect the global cycles of carbon and water. Yet, the detection of these physiological effects of eCO<sub>2</sub> in observational data remains challenging, because natural variations and confounding factors (e.g., warming) can overshadow the eCO<sub>2</sub> effects in observational data of real-world ecosystems. In this study, we aim at developing a method to detect the emergence of the physiological CO<sub>2</sub> effects on various variables related to carbon and water fluxes. We mimic the observational setting in ecosystems using a comprehensive process-based land surface model QUINCY to simulate the leaf-level effects of increasing atmospheric CO<sub>2</sub> concentrations and their century-long propagation through the terrestrial carbon and water cycles across different climate regimes and biomes. We then develop a statistical method based on the signal-to-noise ratio to detect the emergence of the eCO<sub>2</sub> effects. The signal in gross primary production (GPP) emerges at relatively low CO<sub>2</sub> increase (Δ[CO<span>2</span>] ~ 20 ppm) where the leaf area index is relatively high. Compared to GPP, the eCO<sub>2</sub> effect causing reduced transpiration water flux (normalized to leaf area) emerges only at relatively high CO<sub>2</sub> increase (Δ[CO<sub>2</sub>] &gt;&gt; 40 ppm), due to the high sensitivity to climate variability and thus lower signal-to-noise ratio. In general, the response to eCO<sub>2</sub> is detectable earlier for variables of the carbon cycle than the water cycle, when plant productivity is not limited by climatic constraints, and stronger in forest-dominated rather than in grass-dominated ecosystems. Our results provide a step toward when and where we expect to detect physiological CO<sub>2</sub> effects in in-situ flux measurements, how to detect them and encourage future efforts to improve the understanding and quantification of these effects in observations of terrestrial carbon and water dynamics.</p>

opencc-zeroSep 2022View details →
zenodo40/100

A gridded dataset on population densities, real estate prices, transport and land use inside 192 worldwide urban areas

<p>This dataset provides, on a systematic basis, gridded population densities, rents, real estate prices, and transport times (both in<br> public transport and private car) in 192 cities across the world.</p>

opencc-by-4.0Dec 2021View details →
zenodo40/100

Dataset of pollinator functional traits and interaction networks in neotropical mangroves: effects of patch size and surrounding land use

<p>This&nbsp;is the dataset of the manuscript entitled &quot;Pollinator functional traits and interaction networks in neotropical mangroves: effects of patch size and surrounding land use&quot;, which was submitted for publication. The dataset include the functional traits&nbsp;of 162 insect pollinator species and 315&nbsp;interactions with&nbsp;the mangrove species <em>Avicennia germinans, Conocarpus erectus, Laguncularia racemosa,</em> and <em>Rhizophora</em> <em>mangle</em>. The manuscript evaluates the effects of mangrove patch size and surrounding land use on pollinator functional diversity and&nbsp;plant-pollinator interactions in&nbsp;seven mangrove patches from the Colombian Caribbean region.&nbsp;Data variables are&nbsp;pollinator order, family, species,&nbsp;functional traits (pollinator guilds, body size, feeding preference, sociality, and nesting site) and frequency, interacting mangrove species, mangrove patch&nbsp;name,&nbsp;coordinates and&nbsp;size (ha),&nbsp;surrounding land use areas (urban areas, croplands, conserved&nbsp;dry forest, degraded vegetation areas, beach and water) and landscape diversity (Shannon H&#39;).</p>

opencc-by-4.0Sep 2022View details →
zenodo40/100

Fig. 3 in The land snail genus Pincerna Preston, 1907 (Gastropoda: Alycaeidae) from Vietnam and Laos, with description of a new species

Fig. 3. Shells (apertural view, dorsal view, ventral view, and side view) and operculum (outer surface, inner surface, and side view) of Pincerna vanbuensis (Bavay &amp; Dautzenberg, 1900). A, syntype MNHN-IM-2000-31798; B, E, specimen from Thuận Châu, SƠn La, Vietnam, ZMHU; C, specimen from Khoune, Xieng Khouang, Laos, ZMHU; D, specimen from Xiengkho, Houaphanh, Laos, ZMHU.

opencc-by-4.0May 2022View details →
zenodo40/100

Fig. 5 in The land snail genus Pincerna Preston, 1907 (Gastropoda: Alycaeidae) from Vietnam and Laos, with description of a new species

Fig. 5. Details of the shell of Pincerna clausa n. sp. (holotype VNMN-IZ 002.304). A–B, protoconch; C, R2 and sutural tube; D, R3 and boundary between R2 and R3; E, aperture; F, umbilicus.

opencc-by-4.0May 2022View details →
zenodo40/100

Fig. 2 in The land snail genus Pincerna Preston, 1907 (Gastropoda: Alycaeidae) from Vietnam and Laos, with description of a new species

Fig. 2. Shells (apertural view, dorsal view, ventral view, and side view) of Pincerna species. A, Pincerna anceyi (Mabille, 1887), syntype MNHN-IM-2000-31797; B, C, Pincerna mouhoti (L. Pfeiffer, 1862): B, specimen from MƯờng La, SƠn La, Vietnam, ZMHU; C, syntype NHMUK 20170120; D, E, Pincerna costulosus Bavay &amp; Dautzenberg, 1912: D, syntype MNHN-IM-2000-31786; E, specimen from Phong Thổ, Lai Châu, Vietnam, ZMHU.

opencc-by-4.0May 2022View details →
zenodo40/100

Fig. 6 in The land snail genus Pincerna Preston, 1907 (Gastropoda: Alycaeidae) from Vietnam and Laos, with description of a new species

Fig. 6. Synoptic view of Vietnamese and Laos Pincerna species. A, MNHN-IM-2000-31797; B, NHMUK 20170120; C, MNHN- IM-2000-31786; D, VNMN-IZ 002.304; E, MNHN-IM-2000-31798.

opencc-by-4.0May 2022View details →
zenodo40/100

Fig. 4 in The land snail genus Pincerna Preston, 1907 (Gastropoda: Alycaeidae) from Vietnam and Laos, with description of a new species

Fig. 4. Shell (apertural view, dorsal view, ventral view, and side view) of Pincerna clausa, new species. A, holotype VNMN-IZ 002.304; B, C, paratypes ZMHU. MOL 044.

opencc-by-4.0May 2022View details →

ScienceDex guides

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These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.

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Allen Brain Atlas

Allen Brain Atlas is an Allen Institute collection of brain map atlases, datasets, APIs, and analysis tools covering mouse, human, and non-human primate brain resources.

allen-brain-atlas
neuroscienceopenDocumentation, web resources, and API references are available online.
Last verified 2026-04-30Open record

Annotated Behaviour and Observability Dataset (ABODe)

ABODe is a University of Edinburgh DataShare dataset for behavior classification in group-housed mice using home-cage video, identities, bounding boxes, ground-plate positions, and annotator labels.

abode-home-cage
behavioral-neuroscienceopenThe DataShare record exposes download links for annotations, documentation, license text, and the zipped per-snippet data directory.
Last verified 2026-04-30Open record

DANDI Archive for NWB datasets

DANDI is a BRAIN Initiative archive for publishing and sharing neurophysiology data, including electrophysiology, optophysiology, and behavioral data packaged as NWB and related standards.

dandi-nwb
electrophysiologyopenPublished Dandiset metadata and archive endpoints are available through the production DANDI API.
Last verified 2026-04-30Open record

International Brain Laboratory public data

The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.

ibl
behavioral-neuroscienceopenPublic sessions can be searched and loaded from the IBL public data server through ONE.
Last verified 2026-04-29Open record

OpenNeuro

OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.

openneuro
neuroscienceopenPublished datasets are available on demand over the internet.
Last verified 2026-04-29Open record

ScienceDex for faculty

Your academic CV and NIH biosketch

Make your CV in your school's format and your NIH biosketch from it, then download both as Word files.