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Research data keyboard_double_arrow_right Dataset 2021 NetherlandsPublisher:4TU.ResearchData Song, Bingnan; Weijma, Jan; van der Weijden, Renata; Buisman, Cees; Tian, Zilin;Results belonging to paper "High-rate biological selenate reduction in a sequencing batch reactor for recovery of hexagonal selenium".Recovery of selenium (Se) from wastewater provides a solution for both securing Se supply and preventing Se pollution. Here, we developed a high-rate process for biological selenate reduction to elemental selenium. Distinctive from other studies, we aimed for a process with selenate as the main biological electron sink, with minimal formation of methane or sulfide. A sequencing batch reactor, fed with an influent containing 120 mgSe L-1 selenate and ethanol as electron donor and carbon source, was operated for 495 days. The high rates (419 �� 17 mgSe L-1 day-1) were recorded between day 446 and day 495 for a hydraulic retention time of 6h. The maximum conversion efficiency of selenate amounted to 96% with a volumetric conversion rate of 444 mgSe L-1 day-1, which is 6 times higher than the rates reported in the literature thus far. At the end of the experiment, a highly enriched selenate reducing biomass had developed, with a specific activity of 856��26 mgSe-1day-1gbiomass-1, which was nearly 1000-fold higher than that of the inoculum. No evidence was found for the formation of methane, sulfide, or volatile reduced selenium compounds like dimethyl-selenide or H2Se, revealing a high selectivity. Ethanol was incompletely oxidized to acetate. The produced elemental selenium partially accumulated in the reactor as pure (���80% Se of the total mixture of biomass sludge flocs and flaky aggregates, and ~100% of the specific flaky aggregates) selenium black hexagonal needles, with cluster sizes between 20-200 ��m. The new process may serve as the basis for a high-rate technology to remove and recover pure selenium from wastewater or process streams with high selectivity.
4TU.ResearchData | s... arrow_drop_down DANS (Data Archiving and Networked Services)DatasetData sources: DANS (Data Archiving and Networked Services)Smithsonian figshareDataset . 2021License: CC BYData sources: Bielefeld Academic Search Engine (BASE)DANS (Data Archiving and Networked Services)DatasetData sources: DANS (Data Archiving and Networked Services)DANS (Data Archiving and Networked Services)DatasetData sources: DANS (Data Archiving and Networked Services)DANS (Data Archiving and Networked Services)DatasetData sources: DANS (Data Archiving and Networked Services)add ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
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more_vert 4TU.ResearchData | s... arrow_drop_down DANS (Data Archiving and Networked Services)DatasetData sources: DANS (Data Archiving and Networked Services)Smithsonian figshareDataset . 2021License: CC BYData sources: Bielefeld Academic Search Engine (BASE)DANS (Data Archiving and Networked Services)DatasetData sources: DANS (Data Archiving and Networked Services)DANS (Data Archiving and Networked Services)DatasetData sources: DANS (Data Archiving and Networked Services)DANS (Data Archiving and Networked Services)DatasetData sources: DANS (Data Archiving and Networked Services)add ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
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For further information contact us at helpdesk@openaire.euapps Other research productkeyboard_double_arrow_right Other ORP type 2006 NetherlandsPublisher:ECN [etc.] Authors: Reith, H.; Steketee, J.; Brandenburg, W.A.; Sijtsma, L.;Het deelpad Aquatische Biomassa heeft een sterke internationale dimensie. Wereldwijd bestaat een groeiende belangstelling voor het aquatisch milieu (denk hierbij aan waterplanten, zoutwaterlandbouw, micro-algen en zeewieren) als leverancier van voedsel, grondstoffen en energie. Daarnaast is er grote aandacht voor watermanagement, met name gezien de problemen die zich aandienen t.a.v. de berging van regenwater en de beschikbaarheid van zoet water voor drinkwatervoorziening en de landbouw. In dit deelpad worden beide thema’s aan elkaar gekoppeld, zodat meerwaarde ontstaat voor duurzame ontwikkeling met een grote internationale uitstraling van biomassa voor grondstof- en energievoorziening
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For further information contact us at helpdesk@openaire.euResearch data keyboard_double_arrow_right Dataset 2023 NetherlandsPublisher:Zenodo Authors: Kong, Xiangzhen; Determann, Maria; Andersen, Tobias Kuhlmann; Barbosa, Carolina Cerqueira; +6 AuthorsKong, Xiangzhen; Determann, Maria; Andersen, Tobias Kuhlmann; Barbosa, Carolina Cerqueira; Dadi, Tallent; Janssen, Annette B.G.; Paule-Mercado, Ma Cristina; Pujoni, Diego Guimarães Florencio; Schultze, Martin; Rinke, Karsten;This repository contains the dataset linked to the following publication: Article title: Synergistic effects of warming and internal nutrient loading interfere with the long-term stability of lake restoration and induce sudden re-eutrophication Journal: Environmental Science & Technology DOI: 10.1021/acs.est.2c07181 Abstract: Phosphorus (P) precipitation is among the most effective treatments to mitigate lake eutrophication. However, after a period of high effectiveness, studies have shown possible re-eutrophication and the return of harmful algal blooms. While such abrupt ecological changes were attributed to the internal P loading, the role of lake warming and its potential synergistic effects with internal loading, thus far, has been understudied. Here, in a eutrophic lake in central Germany, we quantified the driving mechanisms of the abrupt re-eutrophication and cyanobacterial blooms in 2016 (30 years after the first P precipitation). A process-based lake ecosystem model (GOTM-WET) was established using a high-frequency monitoring dataset covering contrasting trophic states. Model analyses suggested that the internal P release accounted for 68% of the cyanobacterial biomass proliferation, while lake warming contributed to 32%, including direct effects via promoting growth (18%) and synergistic effects via intensifying internal P loading (14%). The model further showed that the synergy was attributed to prolonged lake hypolimnion warming and oxygen depletion. Our study unravels the substantial role of lake warming in promoting cyanobacterial blooms in re-eutrophicated lakes. The warming effects on cyanobacteria via promoting internal loading need more attention in lake management, particularly for urban lakes. SYNOPSIS: Warming synergistically promotes re-eutrophication with internal nutrient loading and exacerbates cyanobacterial blooms in urban lakes 30 years after phosphorus mitigation. Data description by Xiangzhen Kong (xzkong@niglas.ac.cn), 2023-02-20 ---Wet chemical analysis on water samples taken at five depths (0.5, 2.5, 5.0, 7.0 and 9.0 m) from the deepest point in the lake (BA1) at biweekly intervals from 2018.5-2021.8. File name: BAB_BA1_TN_mgL.obs (total nitrogen concentration) BAB_BA1_NH4_mgL.obs (ammonium nitrogen concentration) BAB_BA1_NO3_mgL.obs (nitrate nitrogen concentration) BAB_BA1_TP_mgL.obs (total phosphorus concentration) BAB_BA1_SRP_mgL.obs (Soluble reactive phosphorus concentration) BAB_BA1_DP_mgL.obs (dissolved P concentration) BAB_BA1_DOC_mgL.obs (Dissolved organic carbon concentration) BAB_BA1_Si_mgL.obs (dissolved silicon concentration) BAB_BA1_Chla_HPLC_DIN_mgL.obs (Chl-a concentration) ---CTD probe profile data from the deepest point in the lake (BA1) from 2017.8 to 2021.8 at biweekly basis with approximately 0.1 m vertical resolution File name: t_prof_file_barleber_ctm644.obs (water temperature) oxy_prof_file_barleber_ctm644 (Dissolved oxygen) turb_prof_file_barleber_ctm644.obs (Turbidity) chla_prof_file_barleber_ctm644.obs (Chl-a concentration) ---BBE probe profile data from the deepest point in the lake (BA1) from 2017.8 to 2021.8 at biweekly basis with approximately 0.1 m vertical resolution File name: totalChla_prof_file_barleber_FP2101.obs (Chl-a concentration) bluegreen_prof_file_barleber_FP2101.obs (Blue-green algae Chl-a concentration) green_prof_file_barleber_FP2101.obs (Green algae Chl-a concentration) diatom_prof_file_barleber_FP2101.obs (Diatom Chl-a concentration)
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For further information contact us at helpdesk@openaire.euResearch data keyboard_double_arrow_right Dataset 2017Embargo end date: 07 Aug 2017 NetherlandsPublisher:DANS Data Station Life Sciences van der Sande, M.T.; Arets, E.J.M.M.; Pena Claros, M.; Hoosbeek, M.R.; Caceres-Siani, Yasmani; van der Hout, P.; Poorter, L.;In this study, we test the effects of abiotic factors (light variation, caused by logging disturbance, and soil fertility) and biotic factors (species richness and functional trait composition) on biomass stocks (aboveground biomass, fine root biomass), SOM and productivity in a relatively monodominant Guyanese tropical rainforest. This forest grows on nutrient-poor soils and has few species that contribute most to total abundance. We therefore expected strong effects of soil fertility and species’ traits that determine resource acquisition and conservation, but not of diversity. We evaluated 6 years of data for 30 0.4-ha plots and tested hypotheses using structural equation models. Our results indicate that light availability (through disturbance) and soil fertility – especially P – strongly limit forest biomass productivity and stocks in this Guyanese forest. Low P availability may cause strong environmental filtering, which in turn results in a small set of dominant species. As a result, community trait composition but not species richness determines productivity and stocks of biomass and SOM in tropical forest on poor soils.
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For further information contact us at helpdesk@openaire.euResearch data keyboard_double_arrow_right Dataset 2018 NetherlandsPublisher:Taylor & Francis Authors: Tudorica-Iacobuta, G.; Dubash, Navroz K.; Upadhyaya, Prabhat; Deribe, Mekdelawit; +1 AuthorsTudorica-Iacobuta, G.; Dubash, Navroz K.; Upadhyaya, Prabhat; Deribe, Mekdelawit; Hoehne, N.E.;Global climate change governance has changed substantially in the last decade, with a shift in focus from negotiating globally agreed greenhouse gas (GHG) reduction targets to nationally determined contributions, as enshrined in the 2015 Paris Agreement. This paper analyses trends in adoption of national climate legislation and strategies, GHG targets, and renewable and energy efficiency targets in almost all UNFCCC Parties, focusing on the period from 2007 to 2017. The uniqueness and added value of this paper reside in its broad sweep of countries, the more than decade-long coverage and the use of objective metrics rather than normative judgements. Key results show that national climate legislation and strategies witnessed a strong increase in the first half of the assessed decade, likely due to the political lead up to the Copenhagen Climate Conference in 2009, but have somewhat stagnated in recent years, currently covering 70% of global GHG emissions (almost 50% of countries). In comparison, the coverage of GHG targets increased considerably in the run up to adoption of the Paris Agreement and 89% of global GHG emissions are currently covered by such targets. Renewable energy targets saw a steady spread, with 79% of the global GHG emissions covered in 2017 compared to 45% in 2007, with a steep increase in developing countries. Key policy insightsThe number of countries that have national legislation and strategies in place increased strongly up to 2012, but the increase has levelled off in recent years, now covering 70% of global emissions by 2017 (48% of countries and 76% of global population).Economy-wide GHG reduction targets witnessed a strong increase in the build up to 2015 and are adopted by countries covering 89% of global GHG emissions (76% not counting USA) and 90% of global population (86% not counting USA) in 2017.Renewable energy targets saw a steady increase throughout the last decade with coverage of countries in 2017 comparable to that of GHG targets.Key shifts in national measures coincide with landmark international events – an increase in legislation and strategy in the build-up to the Copenhagen Climate Conference and an increase in targets around the Paris Agreement – emphasizing the importance of the international process to maintaining national momentum. The number of countries that have national legislation and strategies in place increased strongly up to 2012, but the increase has levelled off in recent years, now covering 70% of global emissions by 2017 (48% of countries and 76% of global population). Economy-wide GHG reduction targets witnessed a strong increase in the build up to 2015 and are adopted by countries covering 89% of global GHG emissions (76% not counting USA) and 90% of global population (86% not counting USA) in 2017. Renewable energy targets saw a steady increase throughout the last decade with coverage of countries in 2017 comparable to that of GHG targets. Key shifts in national measures coincide with landmark international events – an increase in legislation and strategy in the build-up to the Copenhagen Climate Conference and an increase in targets around the Paris Agreement – emphasizing the importance of the international process to maintaining national momentum.
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For further information contact us at helpdesk@openaire.euResearch data keyboard_double_arrow_right Dataset 2016 NetherlandsPublisher:ForestPlots.net Cuni-sanchez, Aida; White, Lee J.T.; Calders, K.; Jeffery, Kathryn J.; Abernethy, Katharine; Burt, Andrew; Disney, Mathias; Gilpin, Martin; Gomez-dans, Jose L.; Lewis, Simon L.;Recent studies show widespread encroachment of forest into savannas with important consequences for the global carbon cycle and land-atmosphere interactions. However, little research has focused on in situ measurements of forest-savanna boundary change over time. Using long-term inventory plots we quantify changes in above-ground biomass (AGB), vegetation structure and biodiversity over 20 years for five vegetation types (savanna, colonising forest or F1, successional monodominant forest or F2, Marantaceae forest or F3 and mixed forest or F4) along a savanna-forest transition of central Gabon, all occurring on similar soils. Additionally, we use novel 3D terrestrial laser scanning (TLS) measurements to assess forest structure differences across the transition. Overall, F1 and F2 forests increased in AGB, mainly as a result of adding stems (recruitment in F1) or increased Basal Area (F2). Some plots of F3 and F4 increased in AGB while some decreased. Changes in biodiversity and species’ dominance were small. After 20 years no plot could be classified as having moved to the next stage in the succession. TLS vertical plant profiles showed very distinctive differences amongst the vegetation types. We highlight two relevant points: (i) as forest colonises, changes in biodiversity are much slower than changes in forest structure or AGB; and (ii) all forest types store important quantities of Carbon. Decades long-term monitoring is likely to be required to assess the speed of transition between vegetation types, ideally with TLS, as this provides more objective forest classifications than inventory monitoring.
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For further information contact us at helpdesk@openaire.euResearch data keyboard_double_arrow_right Dataset 2021 NetherlandsPublisher:Zenodo Funded by:ARC | Linkage Projects - Grant ..., ARC | ARC Future Fellowships - ..., ARC | Linkage Projects - Grant ...ARC| Linkage Projects - Grant ID: LP180100159 ,ARC| ARC Future Fellowships - Grant ID: FT190100234 ,ARC| Linkage Projects - Grant ID: LP170101143Keith, David A.; Ferrer-Paris, José R.; Nicholson, Emily; Bishop, Melanie J.; Polidoro, Beth A.; Ramirez-Llodra, Eva; Tozer, Mark G.; Nel, Jeanne L.; Mac Nally, Ralph; Gregr, Edward J.; Watermeyer, Kate E.; Essl, Franz; Faber-Langendoen, Don; Franklin, Janet; Lehmann, Caroline E.R.; Etter, Andrés; Roux, Dirk J.; Stark, Jonathan S.; Rowland, Jessica A.; Brummitt, Neil A.; Fernandez-Arcaya, Ulla C.; Suthers, Iain M.; Wiser, Susan K.; Donohue, Ian; Jackson, Leland J.; Pennington, R.T.; Iliffe, Thomas M.; Gerovasileiou, Vasilis; Giller, Paul; Robson, Belinda J.; Pettorelli, Nathalie; Andrade, Angela; Lindgaard, Arild; Tahvanainen, Teemu; Terauds, Aleks; Chadwick, Michael A.; Murray, Nicholas J.; Moat, Justin; Pliscoff, Patricio; Zager, Irene; Kingsford, Richard T.;This dataset includes the current version of the indicative distribution maps and profiles for Ecosystem Functional Groups - Level 3 of IUCN Global Ecosystem Typology (v2.1). Please refer to Keith et al. (2020) and Keith et al. (2022). The descriptive profiles provide brief summaries of key ecological traits and processes for each functional group of ecosystems to enable any ecosystem type to be assigned to a group. Maps are indicative of global distribution patterns and are not intended to represent fine-scale patterns. The maps show areas of the world containing major (value of 1, coloured red) or minor occurrences (value of 2, coloured yellow) of each ecosystem functional group. Minor occurrences are areas where an ecosystem functional group is scattered in patches within matrices of other ecosystem functional groups or where they occur in substantial areas, but only within a segment of a larger region. Most maps were prepared using a coarse-scale template (e.g. ecoregions), but some were compiled from higher resolution spatial data where available (see details in profiles). Higher resolution mapping is planned in future publications. We emphasise that spatial representation of Ecosystem Functional Groups does not follow higher-order groupings described in respective ecoregion classifications. Consequently, when Ecosystem Functional Groups are aggregated into functional biomes (Level 2 of the Global Ecosystem Typology), spatial patterns may differ from those of biogeographic biomes. Differences reflect the distinctions between functional and biogeographic interpretations of the term, “biome”. The PLuS Alliance supported a workshop in London to initiate development. DAK, EN, RTK, JRFP, JAR & NJM were supported by ARC Linkage Grants LP170101143 and LP180100159 and the MAVA Foundation. The IUCN Commission on Ecosystem Management supported travel for DAK to present aspects of the research to peers and stakeholders at International Congresses on Conservation Biology in 2017 and 2019, and at meetings in Africa, the middle east, and Europe. {"references": ["Keith, David et al. (Eds.) (2020) 'The IUCN Global Ecosystem Typology v2.0: Descriptive profiles for Biomes and Ecosystem Functional Groups'. The International Union for the Conservation of Nature (IUCN), Gland. DOI:10.2305/IUCN.CH.2020.13.en.", "Keith, David et al. (2022) 'A function-based typology for Earth's ecosystems'. Nature DOI:10.1038/s41586-022-05318-4"]}
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For further information contact us at helpdesk@openaire.euResearch data keyboard_double_arrow_right Dataset 2020Embargo end date: 02 Feb 2020 Netherlands, France, FrancePublisher:Harvard Dataverse Zaake, Paul; Paul, Birthe K.; Marshall, Karen; Notenbaert, An; Ouma, Emily; Dione, Michel; Ouma, George O.; Ndambi, Asaah O.;doi: 10.7910/dvn/kpvh8q
handle: 10568/108549
There is limited attention to impacts of climate change on pigs in Uganda by stakeholders, despite the potential vulnerability of pigs to climate change. Pigs are sensitive to heat-stress, as they do not have functioning sweat glands as other livestock species do, and have small lungs which reduces their ability to disseminate heat by panting. The objectives of the study were to i) determine the heat-stress status in pigs, ii) analyze factors influencing heat-stress, and iii) explore the heat-stress adaptation options in Lira District, Uganda. Lira was selected because of presence of both rural & urban areas and expected heat stress throughout the year in the district. The data including household demographics, management systems, age, color, breeds, body/skin temperature, rectal temperature and others were collected from 104 households and 259 pigs during the hot months in Ojwina and Barr sub-counties- Lira district. We collected data on adaptation options during the four gender disaggregated focus group discussions. Weather data was collected during the time of administering the questionnaire, and it was complemented with data from Ngetta Meteorological Station, Lira. STATA, 14
Harvard Dataverse arrow_drop_down DANS (Data Archiving and Networked Services)DatasetData sources: DANS (Data Archiving and Networked Services)CGIAR CGSpace (Consultative Group on International Agricultural Research)Dataset . 2020License: CC BYData sources: Bielefeld Academic Search Engine (BASE)add ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
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more_vert Harvard Dataverse arrow_drop_down DANS (Data Archiving and Networked Services)DatasetData sources: DANS (Data Archiving and Networked Services)CGIAR CGSpace (Consultative Group on International Agricultural Research)Dataset . 2020License: CC BYData sources: Bielefeld Academic Search Engine (BASE)add ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
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For further information contact us at helpdesk@openaire.euResearch data keyboard_double_arrow_right Dataset 2022 NetherlandsPublisher:4TU.ResearchData Authors: Vital, Barbara; Sleutels, Tom; Gagliano, M.C.; Hamelers, Bert;This dataset contains data collected during experiment on foulant fractionation of seawater in reverse electrodialysis (RED). For explanation of the experimental setup we refer you to the published paper. It is being made public both to act as supplementary data for publication and in order for other researchers to use this data in their own work.
4TU.ResearchData | s... arrow_drop_down DANS (Data Archiving and Networked Services)DatasetData sources: DANS (Data Archiving and Networked Services)DANS (Data Archiving and Networked Services)DatasetData sources: DANS (Data Archiving and Networked Services)DANS (Data Archiving and Networked Services)DatasetData sources: DANS (Data Archiving and Networked Services)add ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.4121/20337267&type=result"></script>'); --> </script>
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more_vert 4TU.ResearchData | s... arrow_drop_down DANS (Data Archiving and Networked Services)DatasetData sources: DANS (Data Archiving and Networked Services)DANS (Data Archiving and Networked Services)DatasetData sources: DANS (Data Archiving and Networked Services)DANS (Data Archiving and Networked Services)DatasetData sources: DANS (Data Archiving and Networked Services)add ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.4121/20337267&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.euResearch data keyboard_double_arrow_right Dataset 2017Embargo end date: 27 Jul 2018 NetherlandsPublisher:Dryad Robroek, Bjorn J.M.; Jassey, Vincent E.J.; Payne, Richard J.; Martí, Magalí; Bragazza, Luca; Bleeker, Albert; Buttler, Alexandre; Caporn, Simon J.M.; Dise, Nancy B.; Kattge, Jens; Zajac, Katarzyna; Svensson, Bo H.; van Ruijven, J.; Verhoeven, Jos T.A.;doi: 10.5061/dryad.g1pk3
Environmental dataBioclimatic data and environmental data for all 56 European peatland site (geo referenced by longitude [long], latitude [lat] and altitude [ALT]. MAT = Mean annual temperature (°C), TS = Seasonality in temperature, MAP = Mean annual precipitation (mm), PS = Seasonality in precipitation, tot_sox = Total sulphur deposition SOx (mg m-2 yr-1), tot_noy = Total oxidized nitrogen deposition (mg m-2 yr-1), tot_nhx = Total reduced nitrogen deposition (mg m-2), PT warm = Lang’s moisture index. The four bioclimatic variables (MAT, TS, MAP, PS) were extracted from the WorldClim database (Hijmans, R. J., Cameron, S. E., Parra, J. L., Jones, P. G. & Jarvis, A. Very high resolution interpolated climate surfaces for global land areas. Int. J. Climatol. 25, 1965–1978 (2005)), and averaged over the 2000-2009 period. Atmospheric deposition data were produced using the EMEP (European Monitoring and Evaluation Programme)-based IDEM (Integrated Deposition Model) model (Pieterse, G., Bleeker, A., Vermeulen, A. T., Wu, Y. & Erisman, J. W. High resolution modelling of atmosphere‐canopy exchange of acidifying and eutrophying components and carbon dioxide for European forests. Tellus B 59, 412–424 (2007)) and consisted of grid cell averages of total reduced (NHx) and oxidised (NOy) nitrogen and sulphur (SOx) deposition. The moisture index (PTwarm) was calculated as the ratio between mean precipitation and mean temperature in the warmest quarter (Thornwaite, C. W. & Holzman, B. Measurement of evaporation from land and water surfaces. USDA Technical Bulletin 817, 1–143 (1942))Data 1_environmental data.txtplant community dataAbundance data (% cover) for all vascular plant and bryophyte species from five randomly chosen hummocks and lawns (0.25 m2 quadrats; ten in total) across 56 European Sphagnum-dominated peatlands were collected in two consecutive summers (2010 and 2011). Vascular plants and Sphagnum mosses were identified to the species level. Non-Sphagnum bryophytes were identified to the family level. Lichens were recorded as one group.Data 2_plant community data.txttraits vascular plantsPlant functional traits used to calculate functional indices for the vascular plant communities. Traits were extracted from LEDA (Kleyer, M. et al. The LEDA Traitbase: a database of life‐history traits of the Northwest European flora. J. Ecol. 96, 1266–1274 (2008)). Only trait data available for all species our data-set were extracted.ncomms_Data 3_traits vascular plants.txttraits SphagnumTrait values (means) for Sphagnum spp. C = tissue carbon content (mg g-1), N = tissue nitrogen content (mg g-1), P = tissue phosphorus content (mg g-1), Productivity ( St.w = stem width (mm), l.h.c. = length hyaline cells (µm), w.h.c. = width hyaline cells (µm), l.s.l. = length stem leaves (mm), w.s.l. = width stem leaves. These measured traits were complemented with traits extracted from the literature. These latter traits included plant length (Hill, M. O., Preston, C. D., Bosanquet, S. & Roy, D. B. BRYOATT: attributes of British and Irish mosses, liverworts and hornworts. Centre for Ecology & Hydrology, Huntingdon, UK (2007)), spore diameter and capsule diameter (Sundberg, S., Hansson, J. & Rydin, H. Colonization of Sphagnum on land uplift islands in the Baltic Sea: time, area, distance and life history. Journal of Biogeography 33, 1479–1491 (2006)), productivity (Gunnarsson, U. Global patterns of Sphagnum productivity. J. Bryol. 27, 269–279 (2005))ncomms_Data 4_traits Sphagnum.txt In peatland ecosystems, plant communities mediate a globally significant carbon store. The effects of global environmental change on plant assemblages are expected to be a factor in determining how ecosystem functions such as carbon uptake will respond. Using vegetation data from 56 Sphagnum-dominated peat bogs across Europe, we show that in these ecosystems plant species aggregate into two major clusters that are each defined by shared response to environmental conditions. Across environmental gradients, we find significant taxonomic turnover in both clusters. However, functional identity and functional redundancy of the community as a whole remain unchanged. This strongly suggests that in peat bogs, species turnover across environmental gradients is restricted to functionally similar species. Our results demonstrate that plant taxonomic and functional turnover are decoupled, which may allow these peat bogs to maintain ecosystem functioning when subject to future environmental change.
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visibility 14visibility views 14 download downloads 6 Powered bymore_vert add ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
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Research data keyboard_double_arrow_right Dataset 2021 NetherlandsPublisher:4TU.ResearchData Song, Bingnan; Weijma, Jan; van der Weijden, Renata; Buisman, Cees; Tian, Zilin;Results belonging to paper "High-rate biological selenate reduction in a sequencing batch reactor for recovery of hexagonal selenium".Recovery of selenium (Se) from wastewater provides a solution for both securing Se supply and preventing Se pollution. Here, we developed a high-rate process for biological selenate reduction to elemental selenium. Distinctive from other studies, we aimed for a process with selenate as the main biological electron sink, with minimal formation of methane or sulfide. A sequencing batch reactor, fed with an influent containing 120 mgSe L-1 selenate and ethanol as electron donor and carbon source, was operated for 495 days. The high rates (419 �� 17 mgSe L-1 day-1) were recorded between day 446 and day 495 for a hydraulic retention time of 6h. The maximum conversion efficiency of selenate amounted to 96% with a volumetric conversion rate of 444 mgSe L-1 day-1, which is 6 times higher than the rates reported in the literature thus far. At the end of the experiment, a highly enriched selenate reducing biomass had developed, with a specific activity of 856��26 mgSe-1day-1gbiomass-1, which was nearly 1000-fold higher than that of the inoculum. No evidence was found for the formation of methane, sulfide, or volatile reduced selenium compounds like dimethyl-selenide or H2Se, revealing a high selectivity. Ethanol was incompletely oxidized to acetate. The produced elemental selenium partially accumulated in the reactor as pure (���80% Se of the total mixture of biomass sludge flocs and flaky aggregates, and ~100% of the specific flaky aggregates) selenium black hexagonal needles, with cluster sizes between 20-200 ��m. The new process may serve as the basis for a high-rate technology to remove and recover pure selenium from wastewater or process streams with high selectivity.
4TU.ResearchData | s... arrow_drop_down DANS (Data Archiving and Networked Services)DatasetData sources: DANS (Data Archiving and Networked Services)Smithsonian figshareDataset . 2021License: CC BYData sources: Bielefeld Academic Search Engine (BASE)DANS (Data Archiving and Networked Services)DatasetData sources: DANS (Data Archiving and Networked Services)DANS (Data Archiving and Networked Services)DatasetData sources: DANS (Data Archiving and Networked Services)DANS (Data Archiving and Networked Services)DatasetData sources: DANS (Data Archiving and Networked Services)add ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
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more_vert 4TU.ResearchData | s... arrow_drop_down DANS (Data Archiving and Networked Services)DatasetData sources: DANS (Data Archiving and Networked Services)Smithsonian figshareDataset . 2021License: CC BYData sources: Bielefeld Academic Search Engine (BASE)DANS (Data Archiving and Networked Services)DatasetData sources: DANS (Data Archiving and Networked Services)DANS (Data Archiving and Networked Services)DatasetData sources: DANS (Data Archiving and Networked Services)DANS (Data Archiving and Networked Services)DatasetData sources: DANS (Data Archiving and Networked Services)add ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.4121/12927563&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.euapps Other research productkeyboard_double_arrow_right Other ORP type 2006 NetherlandsPublisher:ECN [etc.] Authors: Reith, H.; Steketee, J.; Brandenburg, W.A.; Sijtsma, L.;Het deelpad Aquatische Biomassa heeft een sterke internationale dimensie. Wereldwijd bestaat een groeiende belangstelling voor het aquatisch milieu (denk hierbij aan waterplanten, zoutwaterlandbouw, micro-algen en zeewieren) als leverancier van voedsel, grondstoffen en energie. Daarnaast is er grote aandacht voor watermanagement, met name gezien de problemen die zich aandienen t.a.v. de berging van regenwater en de beschikbaarheid van zoet water voor drinkwatervoorziening en de landbouw. In dit deelpad worden beide thema’s aan elkaar gekoppeld, zodat meerwaarde ontstaat voor duurzame ontwikkeling met een grote internationale uitstraling van biomassa voor grondstof- en energievoorziening
add ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
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For further information contact us at helpdesk@openaire.euAccess RoutesGreen 0 citations 0 popularity Average influence Average impulse Average Powered by BIP!
more_vert add ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
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For further information contact us at helpdesk@openaire.euResearch data keyboard_double_arrow_right Dataset 2023 NetherlandsPublisher:Zenodo Authors: Kong, Xiangzhen; Determann, Maria; Andersen, Tobias Kuhlmann; Barbosa, Carolina Cerqueira; +6 AuthorsKong, Xiangzhen; Determann, Maria; Andersen, Tobias Kuhlmann; Barbosa, Carolina Cerqueira; Dadi, Tallent; Janssen, Annette B.G.; Paule-Mercado, Ma Cristina; Pujoni, Diego Guimarães Florencio; Schultze, Martin; Rinke, Karsten;This repository contains the dataset linked to the following publication: Article title: Synergistic effects of warming and internal nutrient loading interfere with the long-term stability of lake restoration and induce sudden re-eutrophication Journal: Environmental Science & Technology DOI: 10.1021/acs.est.2c07181 Abstract: Phosphorus (P) precipitation is among the most effective treatments to mitigate lake eutrophication. However, after a period of high effectiveness, studies have shown possible re-eutrophication and the return of harmful algal blooms. While such abrupt ecological changes were attributed to the internal P loading, the role of lake warming and its potential synergistic effects with internal loading, thus far, has been understudied. Here, in a eutrophic lake in central Germany, we quantified the driving mechanisms of the abrupt re-eutrophication and cyanobacterial blooms in 2016 (30 years after the first P precipitation). A process-based lake ecosystem model (GOTM-WET) was established using a high-frequency monitoring dataset covering contrasting trophic states. Model analyses suggested that the internal P release accounted for 68% of the cyanobacterial biomass proliferation, while lake warming contributed to 32%, including direct effects via promoting growth (18%) and synergistic effects via intensifying internal P loading (14%). The model further showed that the synergy was attributed to prolonged lake hypolimnion warming and oxygen depletion. Our study unravels the substantial role of lake warming in promoting cyanobacterial blooms in re-eutrophicated lakes. The warming effects on cyanobacteria via promoting internal loading need more attention in lake management, particularly for urban lakes. SYNOPSIS: Warming synergistically promotes re-eutrophication with internal nutrient loading and exacerbates cyanobacterial blooms in urban lakes 30 years after phosphorus mitigation. Data description by Xiangzhen Kong (xzkong@niglas.ac.cn), 2023-02-20 ---Wet chemical analysis on water samples taken at five depths (0.5, 2.5, 5.0, 7.0 and 9.0 m) from the deepest point in the lake (BA1) at biweekly intervals from 2018.5-2021.8. File name: BAB_BA1_TN_mgL.obs (total nitrogen concentration) BAB_BA1_NH4_mgL.obs (ammonium nitrogen concentration) BAB_BA1_NO3_mgL.obs (nitrate nitrogen concentration) BAB_BA1_TP_mgL.obs (total phosphorus concentration) BAB_BA1_SRP_mgL.obs (Soluble reactive phosphorus concentration) BAB_BA1_DP_mgL.obs (dissolved P concentration) BAB_BA1_DOC_mgL.obs (Dissolved organic carbon concentration) BAB_BA1_Si_mgL.obs (dissolved silicon concentration) BAB_BA1_Chla_HPLC_DIN_mgL.obs (Chl-a concentration) ---CTD probe profile data from the deepest point in the lake (BA1) from 2017.8 to 2021.8 at biweekly basis with approximately 0.1 m vertical resolution File name: t_prof_file_barleber_ctm644.obs (water temperature) oxy_prof_file_barleber_ctm644 (Dissolved oxygen) turb_prof_file_barleber_ctm644.obs (Turbidity) chla_prof_file_barleber_ctm644.obs (Chl-a concentration) ---BBE probe profile data from the deepest point in the lake (BA1) from 2017.8 to 2021.8 at biweekly basis with approximately 0.1 m vertical resolution File name: totalChla_prof_file_barleber_FP2101.obs (Chl-a concentration) bluegreen_prof_file_barleber_FP2101.obs (Blue-green algae Chl-a concentration) green_prof_file_barleber_FP2101.obs (Green algae Chl-a concentration) diatom_prof_file_barleber_FP2101.obs (Diatom Chl-a concentration)
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You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
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more_vert add ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
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For further information contact us at helpdesk@openaire.euResearch data keyboard_double_arrow_right Dataset 2017Embargo end date: 07 Aug 2017 NetherlandsPublisher:DANS Data Station Life Sciences van der Sande, M.T.; Arets, E.J.M.M.; Pena Claros, M.; Hoosbeek, M.R.; Caceres-Siani, Yasmani; van der Hout, P.; Poorter, L.;In this study, we test the effects of abiotic factors (light variation, caused by logging disturbance, and soil fertility) and biotic factors (species richness and functional trait composition) on biomass stocks (aboveground biomass, fine root biomass), SOM and productivity in a relatively monodominant Guyanese tropical rainforest. This forest grows on nutrient-poor soils and has few species that contribute most to total abundance. We therefore expected strong effects of soil fertility and species’ traits that determine resource acquisition and conservation, but not of diversity. We evaluated 6 years of data for 30 0.4-ha plots and tested hypotheses using structural equation models. Our results indicate that light availability (through disturbance) and soil fertility – especially P – strongly limit forest biomass productivity and stocks in this Guyanese forest. Low P availability may cause strong environmental filtering, which in turn results in a small set of dominant species. As a result, community trait composition but not species richness determines productivity and stocks of biomass and SOM in tropical forest on poor soils.
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You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
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more_vert add ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
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For further information contact us at helpdesk@openaire.euResearch data keyboard_double_arrow_right Dataset 2018 NetherlandsPublisher:Taylor & Francis Authors: Tudorica-Iacobuta, G.; Dubash, Navroz K.; Upadhyaya, Prabhat; Deribe, Mekdelawit; +1 AuthorsTudorica-Iacobuta, G.; Dubash, Navroz K.; Upadhyaya, Prabhat; Deribe, Mekdelawit; Hoehne, N.E.;Global climate change governance has changed substantially in the last decade, with a shift in focus from negotiating globally agreed greenhouse gas (GHG) reduction targets to nationally determined contributions, as enshrined in the 2015 Paris Agreement. This paper analyses trends in adoption of national climate legislation and strategies, GHG targets, and renewable and energy efficiency targets in almost all UNFCCC Parties, focusing on the period from 2007 to 2017. The uniqueness and added value of this paper reside in its broad sweep of countries, the more than decade-long coverage and the use of objective metrics rather than normative judgements. Key results show that national climate legislation and strategies witnessed a strong increase in the first half of the assessed decade, likely due to the political lead up to the Copenhagen Climate Conference in 2009, but have somewhat stagnated in recent years, currently covering 70% of global GHG emissions (almost 50% of countries). In comparison, the coverage of GHG targets increased considerably in the run up to adoption of the Paris Agreement and 89% of global GHG emissions are currently covered by such targets. Renewable energy targets saw a steady spread, with 79% of the global GHG emissions covered in 2017 compared to 45% in 2007, with a steep increase in developing countries. Key policy insightsThe number of countries that have national legislation and strategies in place increased strongly up to 2012, but the increase has levelled off in recent years, now covering 70% of global emissions by 2017 (48% of countries and 76% of global population).Economy-wide GHG reduction targets witnessed a strong increase in the build up to 2015 and are adopted by countries covering 89% of global GHG emissions (76% not counting USA) and 90% of global population (86% not counting USA) in 2017.Renewable energy targets saw a steady increase throughout the last decade with coverage of countries in 2017 comparable to that of GHG targets.Key shifts in national measures coincide with landmark international events – an increase in legislation and strategy in the build-up to the Copenhagen Climate Conference and an increase in targets around the Paris Agreement – emphasizing the importance of the international process to maintaining national momentum. The number of countries that have national legislation and strategies in place increased strongly up to 2012, but the increase has levelled off in recent years, now covering 70% of global emissions by 2017 (48% of countries and 76% of global population). Economy-wide GHG reduction targets witnessed a strong increase in the build up to 2015 and are adopted by countries covering 89% of global GHG emissions (76% not counting USA) and 90% of global population (86% not counting USA) in 2017. Renewable energy targets saw a steady increase throughout the last decade with coverage of countries in 2017 comparable to that of GHG targets. Key shifts in national measures coincide with landmark international events – an increase in legislation and strategy in the build-up to the Copenhagen Climate Conference and an increase in targets around the Paris Agreement – emphasizing the importance of the international process to maintaining national momentum.
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You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
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You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
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For further information contact us at helpdesk@openaire.euResearch data keyboard_double_arrow_right Dataset 2016 NetherlandsPublisher:ForestPlots.net Cuni-sanchez, Aida; White, Lee J.T.; Calders, K.; Jeffery, Kathryn J.; Abernethy, Katharine; Burt, Andrew; Disney, Mathias; Gilpin, Martin; Gomez-dans, Jose L.; Lewis, Simon L.;Recent studies show widespread encroachment of forest into savannas with important consequences for the global carbon cycle and land-atmosphere interactions. However, little research has focused on in situ measurements of forest-savanna boundary change over time. Using long-term inventory plots we quantify changes in above-ground biomass (AGB), vegetation structure and biodiversity over 20 years for five vegetation types (savanna, colonising forest or F1, successional monodominant forest or F2, Marantaceae forest or F3 and mixed forest or F4) along a savanna-forest transition of central Gabon, all occurring on similar soils. Additionally, we use novel 3D terrestrial laser scanning (TLS) measurements to assess forest structure differences across the transition. Overall, F1 and F2 forests increased in AGB, mainly as a result of adding stems (recruitment in F1) or increased Basal Area (F2). Some plots of F3 and F4 increased in AGB while some decreased. Changes in biodiversity and species’ dominance were small. After 20 years no plot could be classified as having moved to the next stage in the succession. TLS vertical plant profiles showed very distinctive differences amongst the vegetation types. We highlight two relevant points: (i) as forest colonises, changes in biodiversity are much slower than changes in forest structure or AGB; and (ii) all forest types store important quantities of Carbon. Decades long-term monitoring is likely to be required to assess the speed of transition between vegetation types, ideally with TLS, as this provides more objective forest classifications than inventory monitoring.
add ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.5521/forestplots.net/2016_1&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.eu1 citations 1 popularity Average influence Average impulse Average Powered by BIP!
more_vert add ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.5521/forestplots.net/2016_1&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.euResearch data keyboard_double_arrow_right Dataset 2021 NetherlandsPublisher:Zenodo Funded by:ARC | Linkage Projects - Grant ..., ARC | ARC Future Fellowships - ..., ARC | Linkage Projects - Grant ...ARC| Linkage Projects - Grant ID: LP180100159 ,ARC| ARC Future Fellowships - Grant ID: FT190100234 ,ARC| Linkage Projects - Grant ID: LP170101143Keith, David A.; Ferrer-Paris, José R.; Nicholson, Emily; Bishop, Melanie J.; Polidoro, Beth A.; Ramirez-Llodra, Eva; Tozer, Mark G.; Nel, Jeanne L.; Mac Nally, Ralph; Gregr, Edward J.; Watermeyer, Kate E.; Essl, Franz; Faber-Langendoen, Don; Franklin, Janet; Lehmann, Caroline E.R.; Etter, Andrés; Roux, Dirk J.; Stark, Jonathan S.; Rowland, Jessica A.; Brummitt, Neil A.; Fernandez-Arcaya, Ulla C.; Suthers, Iain M.; Wiser, Susan K.; Donohue, Ian; Jackson, Leland J.; Pennington, R.T.; Iliffe, Thomas M.; Gerovasileiou, Vasilis; Giller, Paul; Robson, Belinda J.; Pettorelli, Nathalie; Andrade, Angela; Lindgaard, Arild; Tahvanainen, Teemu; Terauds, Aleks; Chadwick, Michael A.; Murray, Nicholas J.; Moat, Justin; Pliscoff, Patricio; Zager, Irene; Kingsford, Richard T.;This dataset includes the current version of the indicative distribution maps and profiles for Ecosystem Functional Groups - Level 3 of IUCN Global Ecosystem Typology (v2.1). Please refer to Keith et al. (2020) and Keith et al. (2022). The descriptive profiles provide brief summaries of key ecological traits and processes for each functional group of ecosystems to enable any ecosystem type to be assigned to a group. Maps are indicative of global distribution patterns and are not intended to represent fine-scale patterns. The maps show areas of the world containing major (value of 1, coloured red) or minor occurrences (value of 2, coloured yellow) of each ecosystem functional group. Minor occurrences are areas where an ecosystem functional group is scattered in patches within matrices of other ecosystem functional groups or where they occur in substantial areas, but only within a segment of a larger region. Most maps were prepared using a coarse-scale template (e.g. ecoregions), but some were compiled from higher resolution spatial data where available (see details in profiles). Higher resolution mapping is planned in future publications. We emphasise that spatial representation of Ecosystem Functional Groups does not follow higher-order groupings described in respective ecoregion classifications. Consequently, when Ecosystem Functional Groups are aggregated into functional biomes (Level 2 of the Global Ecosystem Typology), spatial patterns may differ from those of biogeographic biomes. Differences reflect the distinctions between functional and biogeographic interpretations of the term, “biome”. The PLuS Alliance supported a workshop in London to initiate development. DAK, EN, RTK, JRFP, JAR & NJM were supported by ARC Linkage Grants LP170101143 and LP180100159 and the MAVA Foundation. The IUCN Commission on Ecosystem Management supported travel for DAK to present aspects of the research to peers and stakeholders at International Congresses on Conservation Biology in 2017 and 2019, and at meetings in Africa, the middle east, and Europe. {"references": ["Keith, David et al. (Eds.) (2020) 'The IUCN Global Ecosystem Typology v2.0: Descriptive profiles for Biomes and Ecosystem Functional Groups'. The International Union for the Conservation of Nature (IUCN), Gland. DOI:10.2305/IUCN.CH.2020.13.en.", "Keith, David et al. (2022) 'A function-based typology for Earth's ecosystems'. Nature DOI:10.1038/s41586-022-05318-4"]}
add ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.5281/zenodo.10081251&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.eu1 citations 1 popularity Average influence Average impulse Average Powered by BIP!
more_vert add ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.5281/zenodo.10081251&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.euResearch data keyboard_double_arrow_right Dataset 2020Embargo end date: 02 Feb 2020 Netherlands, France, FrancePublisher:Harvard Dataverse Zaake, Paul; Paul, Birthe K.; Marshall, Karen; Notenbaert, An; Ouma, Emily; Dione, Michel; Ouma, George O.; Ndambi, Asaah O.;doi: 10.7910/dvn/kpvh8q
handle: 10568/108549
There is limited attention to impacts of climate change on pigs in Uganda by stakeholders, despite the potential vulnerability of pigs to climate change. Pigs are sensitive to heat-stress, as they do not have functioning sweat glands as other livestock species do, and have small lungs which reduces their ability to disseminate heat by panting. The objectives of the study were to i) determine the heat-stress status in pigs, ii) analyze factors influencing heat-stress, and iii) explore the heat-stress adaptation options in Lira District, Uganda. Lira was selected because of presence of both rural & urban areas and expected heat stress throughout the year in the district. The data including household demographics, management systems, age, color, breeds, body/skin temperature, rectal temperature and others were collected from 104 households and 259 pigs during the hot months in Ojwina and Barr sub-counties- Lira district. We collected data on adaptation options during the four gender disaggregated focus group discussions. Weather data was collected during the time of administering the questionnaire, and it was complemented with data from Ngetta Meteorological Station, Lira. STATA, 14
Harvard Dataverse arrow_drop_down DANS (Data Archiving and Networked Services)DatasetData sources: DANS (Data Archiving and Networked Services)CGIAR CGSpace (Consultative Group on International Agricultural Research)Dataset . 2020License: CC BYData sources: Bielefeld Academic Search Engine (BASE)add ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.7910/dvn/kpvh8q&type=result"></script>'); --> </script>
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more_vert Harvard Dataverse arrow_drop_down DANS (Data Archiving and Networked Services)DatasetData sources: DANS (Data Archiving and Networked Services)CGIAR CGSpace (Consultative Group on International Agricultural Research)Dataset . 2020License: CC BYData sources: Bielefeld Academic Search Engine (BASE)add ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.7910/dvn/kpvh8q&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.euResearch data keyboard_double_arrow_right Dataset 2022 NetherlandsPublisher:4TU.ResearchData Authors: Vital, Barbara; Sleutels, Tom; Gagliano, M.C.; Hamelers, Bert;This dataset contains data collected during experiment on foulant fractionation of seawater in reverse electrodialysis (RED). For explanation of the experimental setup we refer you to the published paper. It is being made public both to act as supplementary data for publication and in order for other researchers to use this data in their own work.
4TU.ResearchData | s... arrow_drop_down DANS (Data Archiving and Networked Services)DatasetData sources: DANS (Data Archiving and Networked Services)DANS (Data Archiving and Networked Services)DatasetData sources: DANS (Data Archiving and Networked Services)DANS (Data Archiving and Networked Services)DatasetData sources: DANS (Data Archiving and Networked Services)add ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.4121/20337267&type=result"></script>'); --> </script>
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more_vert 4TU.ResearchData | s... arrow_drop_down DANS (Data Archiving and Networked Services)DatasetData sources: DANS (Data Archiving and Networked Services)DANS (Data Archiving and Networked Services)DatasetData sources: DANS (Data Archiving and Networked Services)DANS (Data Archiving and Networked Services)DatasetData sources: DANS (Data Archiving and Networked Services)add ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.4121/20337267&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.euResearch data keyboard_double_arrow_right Dataset 2017Embargo end date: 27 Jul 2018 NetherlandsPublisher:Dryad Robroek, Bjorn J.M.; Jassey, Vincent E.J.; Payne, Richard J.; Martí, Magalí; Bragazza, Luca; Bleeker, Albert; Buttler, Alexandre; Caporn, Simon J.M.; Dise, Nancy B.; Kattge, Jens; Zajac, Katarzyna; Svensson, Bo H.; van Ruijven, J.; Verhoeven, Jos T.A.;doi: 10.5061/dryad.g1pk3
Environmental dataBioclimatic data and environmental data for all 56 European peatland site (geo referenced by longitude [long], latitude [lat] and altitude [ALT]. MAT = Mean annual temperature (°C), TS = Seasonality in temperature, MAP = Mean annual precipitation (mm), PS = Seasonality in precipitation, tot_sox = Total sulphur deposition SOx (mg m-2 yr-1), tot_noy = Total oxidized nitrogen deposition (mg m-2 yr-1), tot_nhx = Total reduced nitrogen deposition (mg m-2), PT warm = Lang’s moisture index. The four bioclimatic variables (MAT, TS, MAP, PS) were extracted from the WorldClim database (Hijmans, R. J., Cameron, S. E., Parra, J. L., Jones, P. G. & Jarvis, A. Very high resolution interpolated climate surfaces for global land areas. Int. J. Climatol. 25, 1965–1978 (2005)), and averaged over the 2000-2009 period. Atmospheric deposition data were produced using the EMEP (European Monitoring and Evaluation Programme)-based IDEM (Integrated Deposition Model) model (Pieterse, G., Bleeker, A., Vermeulen, A. T., Wu, Y. & Erisman, J. W. High resolution modelling of atmosphere‐canopy exchange of acidifying and eutrophying components and carbon dioxide for European forests. Tellus B 59, 412–424 (2007)) and consisted of grid cell averages of total reduced (NHx) and oxidised (NOy) nitrogen and sulphur (SOx) deposition. The moisture index (PTwarm) was calculated as the ratio between mean precipitation and mean temperature in the warmest quarter (Thornwaite, C. W. & Holzman, B. Measurement of evaporation from land and water surfaces. USDA Technical Bulletin 817, 1–143 (1942))Data 1_environmental data.txtplant community dataAbundance data (% cover) for all vascular plant and bryophyte species from five randomly chosen hummocks and lawns (0.25 m2 quadrats; ten in total) across 56 European Sphagnum-dominated peatlands were collected in two consecutive summers (2010 and 2011). Vascular plants and Sphagnum mosses were identified to the species level. Non-Sphagnum bryophytes were identified to the family level. Lichens were recorded as one group.Data 2_plant community data.txttraits vascular plantsPlant functional traits used to calculate functional indices for the vascular plant communities. Traits were extracted from LEDA (Kleyer, M. et al. The LEDA Traitbase: a database of life‐history traits of the Northwest European flora. J. Ecol. 96, 1266–1274 (2008)). Only trait data available for all species our data-set were extracted.ncomms_Data 3_traits vascular plants.txttraits SphagnumTrait values (means) for Sphagnum spp. C = tissue carbon content (mg g-1), N = tissue nitrogen content (mg g-1), P = tissue phosphorus content (mg g-1), Productivity ( St.w = stem width (mm), l.h.c. = length hyaline cells (µm), w.h.c. = width hyaline cells (µm), l.s.l. = length stem leaves (mm), w.s.l. = width stem leaves. These measured traits were complemented with traits extracted from the literature. These latter traits included plant length (Hill, M. O., Preston, C. D., Bosanquet, S. & Roy, D. B. BRYOATT: attributes of British and Irish mosses, liverworts and hornworts. Centre for Ecology & Hydrology, Huntingdon, UK (2007)), spore diameter and capsule diameter (Sundberg, S., Hansson, J. & Rydin, H. Colonization of Sphagnum on land uplift islands in the Baltic Sea: time, area, distance and life history. Journal of Biogeography 33, 1479–1491 (2006)), productivity (Gunnarsson, U. Global patterns of Sphagnum productivity. J. Bryol. 27, 269–279 (2005))ncomms_Data 4_traits Sphagnum.txt In peatland ecosystems, plant communities mediate a globally significant carbon store. The effects of global environmental change on plant assemblages are expected to be a factor in determining how ecosystem functions such as carbon uptake will respond. Using vegetation data from 56 Sphagnum-dominated peat bogs across Europe, we show that in these ecosystems plant species aggregate into two major clusters that are each defined by shared response to environmental conditions. Across environmental gradients, we find significant taxonomic turnover in both clusters. However, functional identity and functional redundancy of the community as a whole remain unchanged. This strongly suggests that in peat bogs, species turnover across environmental gradients is restricted to functionally similar species. Our results demonstrate that plant taxonomic and functional turnover are decoupled, which may allow these peat bogs to maintain ecosystem functioning when subject to future environmental change.
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You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
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visibility 14visibility views 14 download downloads 6 Powered bymore_vert add ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.5061/dryad.g1pk3&type=result"></script>'); --> </script>
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