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Wheat Biomass for Kherson and Poltava regions in Ukraine The dataset contains Dry Above Ground Biomass (DAM) estimates over the Kherson and Poltava regions in Ukraine for years 2020,2021 and 2022. - Processing:The processing is done using the AgriCarbon-EOv1.5 processing chain, using the TREX processing centre at CNES France.The input remote sensing data are L2A Sentinel-2 surface reflectances provided by the MAJA processing chain based on the Copernicus Sentinel-2 L1C data.The Landcover maps are provided using ML Deep learning based on the Copernicus L2A data.The daily weather data is extracted from ERA5Land products (C3S). -Geophysical variable:Dry Above ground biomass of winter wheat in g/m2. - Extents: * DAM estimates over the Copernicus Sentinel-2 tile 36TWT cover the Kherson region.* DAM estimates over the Copernicus Sentinel-2 tile 36UVA cover the Poltava region. - Spatial resolution:10m resolution estimlates over wheat plots identified in the landcover map. - Temporal coverage:Estimates are provided at the end of the wheat cycle for cycles:* The year 2020 correspond to cycle: 2019-2020* The year 2021 corresponds to cycle : 2020-2021* The year 2022 corresponds to cycle : 2021-2022 - Projection: EPSG:32636 - File content: Each Raster file has 2 bands containing respectively: * band1: mean value of DAM in g/m2. * band2: standard deviation of DAM in g/m2. - List of maps:* Dry_aboveground_biomass_2020_T36TWT_Kherson_Ukraine.tif* Dry_aboveground_biomass_2020_T36UVA_Poltava_Ukraine.tif* Dry_aboveground_biomass_2021_T36TWT_Kherson_Ukraine.tif* Dry_aboveground_biomass_2021_T36UVA_Poltava_Ukraine.tif* Dry_aboveground_biomass_2022_T36TWT_Kherson_Ukraine.tif* Dry_aboveground_biomass_2022_T36UVA_Poltava_Ukraine.tif

The Global Yield Gap Atlas project (GYGA - http://yieldgap.org ) has undertaken a yield gap assessment following the protocol recommended by van Ittersum et. al. (van Ittersum et. al., 2013). This datafile holds the results for rainfed rice.

Abstract Background The ascomycete fungus Podospora anserina has been appreciated for its targeted carbohydrate-active enzymatic arsenal. As a late colonizer of herbivorous dung, the fungus acts specifically on the more recalcitrant fraction of lignocellulose and this lignin-rich biotope might have resulted in the evolution of ligninolytic activities. However, the lignin-degrading abilities of the fungus have not been demonstrated by chemical analyses at the molecular level and are, thus far, solely based on genome and secretome predictions. To evaluate whether P. anserina might provide a novel source of lignin-active enzymes to tap into for potential biotechnological applications, we comprehensively mapped wheat straw lignin during fungal growth and characterized the fungal secretome. Results Quantitative 13C lignin internal standard py-GC–MS analysis showed substantial lignin removal during the 7 days of fungal growth (24% w/w), though carbohydrates were preferably targeted (58% w/w removal). Structural characterization of residual lignin by using py-GC–MS and HSQC NMR analyses demonstrated that Cα-oxidized substructures significantly increased through fungal action, while intact β-O-4′ aryl ether linkages, p-coumarate and ferulate moieties decreased, albeit to lesser extents than observed for the action of basidiomycetes. Proteomic analysis indicated that the presence of lignin induced considerable changes in the secretome of P. anserina. This was particularly reflected in a strong reduction of cellulases and galactomannanases, while H2O2-producing enzymes clearly increased. The latter enzymes, together with laccases, were likely involved in the observed ligninolysis. Conclusions For the first time, we provide unambiguous evidence for the ligninolytic activity of the ascomycete fungus P. anserina and expand the view on its enzymatic repertoire beyond carbohydrate degradation. Our results can be of significance for the development of biological lignin conversion technologies by contributing to the quest for novel lignin-active enzymes and organisms. Background The ascomycete fungus Podospora anserina has been appreciated for its targeted carbohydrate-active enzymatic arsenal. As a late colonizer of herbivorous dung, the fungus acts specifically on the more recalcitrant fraction of lignocellulose and this lignin-rich biotope might have resulted in the evolution of ligninolytic activities. However, the lignin-degrading abilities of the fungus have not been demonstrated by chemical analyses at the molecular level and are, thus far, solely based on genome and secretome predictions. To evaluate whether P. anserina might provide a novel source of lignin-active enzymes to tap into for potential biotechnological applications, we comprehensively mapped wheat straw lignin during fungal growth and characterized the fungal secretome. Results Quantitative 13C lignin internal standard py-GC–MS analysis showed substantial lignin removal during the 7 days of fungal growth (24% w/w), though carbohydrates were preferably targeted (58% w/w removal). Structural characterization of residual lignin by using py-GC–MS and HSQC NMR analyses demonstrated that Cα-oxidized substructures significantly increased through fungal action, while intact β-O-4′ aryl ether linkages, p-coumarate and ferulate moieties decreased, albeit to lesser extents than observed for the action of basidiomycetes. Proteomic analysis indicated that the presence of lignin induced considerable changes in the secretome of P. anserina. This was particularly reflected in a strong reduction of cellulases and galactomannanases, while H2O2-producing enzymes clearly increased. The latter enzymes, together with laccases, were likely involved in the observed ligninolysis. Conclusions For the first time, we provide unambiguous evidence for the ligninolytic activity of the ascomycete fungus P. anserina and expand the view on its enzymatic repertoire beyond carbohydrate degradation. Our results can be of significance for the development of biological lignin conversion technologies by contributing to the quest for novel lignin-active enzymes and organisms.

This dataset contains files produced for and generated from the CCAFS Household Baseline Study carried out in sites in Latin America (Trifinio in Honduras/Guatemala, and Cauca in Colombia) and in South-East Asia (a site in each of Cambodia, Laos and Vietnam) in the latter months of 2014 and the early months of 2015. There are six sites in all (two sites from Trifinio). Before downloading any of the files, particularly the data files, please download and read the CCAFS ReadMe file which is prefixed by the code 0000. To gain access to the GPS coordinates from the restricted files please download and complete the Non-disclosure agreement from the file "0002 Non-Disclosure Agreement 2013-01-20.pdf" and send this to Wiebke Foerch at w.foerch@cgiar.org The study was based on earlier baseline studies carried out in sites in West and East Africa and in South Asia. Data and other files from these earlier studies are available in a separate dataset in this Dataverse archive. (CCAFS Household Baseline Survey 2010-2012). If you are intending to use data from both studies together we suggest you read the file "0001 Questionnaire Differences & Recoding Details 2015-10-29.pdf" which explains differences between the two studies.

The Global Yield Gap Atlas project (GYGA - http://yieldgap.org ) has undertaken a yield gap assessment following the protocol recommended by van Ittersum et. al. (van Ittersum et. al., 2013). This datafile holds the results for rainfed sugarcane.

This dataset gathers data used to determine the temporal variability of couplings between pelagic and benthic habitats for fish assemblages at five periods. Organic matter fluxes were assessed using stable isotopes analysis. Species relative biomass was considered to explore energy fluxes within the fish assemblage

The dataset covers biotic and abiotic data from the aquatic habitat of a population of the sediment-rooted macrophyte Myriophyllum spicatum in the temperate climate region (The Netherlands). The growth of M. spicatum was monitored in 0.2025 m2 plant baskets installed in an experimental ditch. Parameters monitored included biomass (fresh and dry weight), shoot length, seasonal short-term growth rates of shoots, relevant environmental parameters and weather data. This dataset includes the 2-year experimental biotic (macrophyte biomass and growth data) and environmental data (water quality data, sediment data). A second file includes the statistical data. A third file includes the weather data.

Aromatization of furan and substituted furans over zeolite catalysts is a promising reaction to convert cellulose-derived compounds into valuable aromatic hydrocarbons and light olefins. A lack of understanding of the reaction mechanism however hinders further development of this process. Here, we propose the reaction mechanism, underlying the chemistry of furan and methanol co-aromatization over HZSM-5 zeolite catalyst. Applying 13C isotope labeling in a combination with NMR spectroscopy and high temporal resolution gas chromatography-mass spectrometry analysis, we demonstrate that aromatization of furan and methanol are not mechanistically separated and can be described within the dual-cycle hydrocarbon pool mechanism. Cofeeding furan with methanol leads to a significant enhancement of light aromatics selectivity and increased catalyst lifetime.