Skip to Main Content

Accession details

Passport data details

Download

Last update

Characterisation and evaluation data

Experiment descriptionTrait nameTrait methodScoreScore link
Field trial of 385 natura[...] ADF_04_17Acid detergent fiber (ADF[...] 15.4016337271
Field trial of 385 natura[...] ADF_10_17Acid detergent fiber (ADF[...] 23.12326251271
Field trial of 385 natura[...] ADL_04_17Acid Detergent Lignin (AD[...] 0.44948757271
Field trial of 385 natura[...] ADL_10_17Acid Detergent Lignin (AD[...] 1.9029012350000001271
Field trial of 385 natura[...] AHD_16Aftermath heading in 2016[...] 1.211114757271
Field trial of 385 natura[...] AHD_16Aftermath heading in 2016[...] 4.0988205210000004271
Field trial of 385 natura[...] AHD_16Aftermath heading in 2016[...] 3.7453283709999998271
Field trial of 385 natura[...] AHD_17Aftermath heading in 2017[...] 2.3180506150000002271
Field trial of 385 natura[...] AHD_17Aftermath heading in 2017[...] 4.4950778519999997271
Field trial of 385 natura[...] AHD_17Aftermath heading in 2017[...] 1.065276007271
Field trial of 385 natura[...] AMH_17Autumn canopy height in 2[...] 112.7994894271
Field trial of 385 natura[...] AMH_17Autumn canopy height in 2[...] 121.59681569999999271
Field trial of 385 natura[...] CH300h_16Canopy height at 300 grow[...] 150.04638969999999271
Field trial of 385 natura[...] CH300h_16Canopy height at 300 grow[...] 246.4839695271
Field trial of 385 natura[...] CH300h_17Canopy height at 300 grow[...] 134.63473999999999271
Field trial of 385 natura[...] CH300h_17Canopy height at 300 grow[...] 147.8585732271
Field trial of 385 natura[...] CH400h_16Canopy height at 400 grow[...] 112.9655353271
Field trial of 385 natura[...] CH400h_16Canopy height at 400 grow[...] 190.12717520000001271
Field trial of 385 natura[...] CH400h_17Canopy height at 400 grow[...] 114.090975271
Field trial of 385 natura[...] CH400h_17Canopy height at 400 grow[...] 115.6156482271
Field trial of 385 natura[...] CHs300_16Canopy height at 300 grow[...] 194.5938471271
Field trial of 385 natura[...] CHs300_16Canopy height at 300 grow[...] 51.316421220000002271
Field trial of 385 natura[...] CHs300_16Canopy height at 300 grow[...] 23.077682459999998271
Field trial of 385 natura[...] CHs300_17Canopy height at 300 grow[...] 73.341266020000006271
Field trial of 385 natura[...] CHs300_17Canopy height at 300 grow[...] 45.649190310000002271
Field trial of 385 natura[...] CHs300_17Canopy height at 300 grow[...] 48.504018709999997271
Field trial of 385 natura[...] CHs500_16Canopy height at 500 grow[...] 90.197943280000004271
Field trial of 385 natura[...] CHs500_16Canopy height at 500 grow[...] 84.437492349999999271
Field trial of 385 natura[...] CHs500_17Canopy height at 500 grow[...] 88.665063669999995271
Field trial of 385 natura[...] CHs500_17Canopy height at 500 grow[...] 128.77490610000001271
Field trial of 385 natura[...] CHs500_17Canopy height at 500 grow[...] 71.177458430000001271
Field trial of 385 natura[...] DES_2015Days from sowing to emerg[...] 26.625928569999999271
Field trial of 385 natura[...] DHE_01_16Drechslera spp. (Syn. Hel[...] 4.8919815271
Field trial of 385 natura[...] DHE_04_17Drechslera spp. (Syn. Hel[...] 3.8543533239999999271
Field trial of 385 natura[...] DHE_07_16Drechslera spp. (Syn. Hel[...] 3.7318172700000001271
Field trial of 385 natura[...] DIS_15Susceptibility to indeter[...] 4.1888145080000001271
Field trial of 385 natura[...] DIS_15Susceptibility to indeter[...] 2.9753393739999998271
Field trial of 385 natura[...] DIS_16Susceptibility to indeter[...] 2.2763928290000002271
Field trial of 385 natura[...] DIS_16Susceptibility to indeter[...] 1.3463221839999999271
Field trial of 385 natura[...] DIS_17Susceptibility to indeter[...] 3.9552202630000002271
Field trial of 385 natura[...] DIS_17Susceptibility to indeter[...] 4.2325286719999999271
Field trial of 385 natura[...] DIS_17Susceptibility to indeter[...] 3.267542105271
Field trial of 385 natura[...] DNDF_04_17In vitro neutral detergen[...] 81.410251610000003271
Field trial of 385 natura[...] DNDF_10_17In vitro neutral detergen[...] 71.518518520000001271
Field trial of 385 natura[...] DRBBlack rust (Puccinia gram[...] 3.6203160429999999271
Field trial of 385 natura[...] DRO_16Drought stress symptoms i[...] 6.3923558229999999271
Field trial of 385 natura[...] DRO_16Drought stress symptoms i[...] 6.3517110140000002271
Field trial of 385 natura[...] DST_17Density of elongated fert[...] 7.7665761800000004271
Field trial of 385 natura[...] DST_17Density of elongated fert[...] 7.0511938230000002271
Field trial of 385 natura[...] DVG_17Sward density in April 20[...] 4.8919815271
  • 1 - 50

Experiment details

Experiment desciptionDataset remarkExperiment start yearExperiment end yearExperiment report
Field trial of 385 natural populations and 12 cultivars of perennial ryegrass at Poel Island (IPK) in Germany (53.990 lat, 11.468 lon). The trial was sown on 8th of April 2015. Each population or cultivar was sown in three 1m² micro-swards with 2g, 4g or 6g seeds according to whether its previously checked germination rate was higher than 80%, between 80 and 60%, or smaller than 60%, respectively. The populations and cultivars were sown in three complete blocks (replicates). The trial was monitored until end of 2017. Micro-swards were cut (all aerial biomass higher than 7 cm above ground surface) regularly as to simulate common cutting regime of meadows used for green forage production or grazing. Anti-dicotyledon herbicide was applied once in 2015 and a second time in 2016. A nitrogen fertilization was applied with 60 kg N ha-1 two months after sowing and after each aerial biomass cut and with 80 kg N ha-1 after winters 2015-2016 and 2016-2017 at start of spring growth. In this location, drought stress remained small or negligible during both summers 2016 and 2017. However, the winter periods were colder (mean temperature below 3°C) than in the two other locations, especially at the end of the 2015-2016 winter period. The 12 cultivars used as controls were AberAvon, AberDart, Aurora, Barutti, Clerpin, Fennema, Lipresso, Mara, Meloni, Merks, Premium and Vigor.These C&E data were recorded in the frame of the project GrassLandscape (2015-2019) awarded by the FACCE-JPI ERA-NET+ call `Climate Smart Agriculture¿ (consortium: INRAE and EPHE in France, IPK in Germany, IBERS in the UK, ILVO in Belgium, project coordinator: JP Sampoux, INRAE). This project intended to discover climate adaptive genomic diversity in natural populations of perennial ryegrass and to relate adaptive loci to climate constraints and adaptive phenotypes. This project involved 385 natural populations of perennial ryegrass and 11 natural populations from related species originating from various regions of Europe and the Near-East. These populations were maintained as accessions in 15 genebanks of the ECPGR network and the USDA GRIN which provided seed samples. 14 perennial ryegrass cultivars were additionally used as checks. All accessions and cultivars were phenotyped for C&E data in three locations in Germany (IPK, Poel), Belgium(ILVO, Melle) and France (INRAE, Lusignan) from 2015 to 2017 or 2018 (according to location) and were genotyped for 507 583 SNP loci. The project identified 633 loci putatively involved in climate adaptation, among which 374 were positioned within or close to a gene. Papers published in the frame of the GrassLandscape project: Blanco-Pastor, J. L. et al. (2019), Journal of Biogeography (46), 1451-1465. , doi: 10.1111/jbi.13587; Keep, T. et al. (2020), Genes|Genomes|Genetics, doi:10.1534/g3.120.401491; Blanco-Pastor, J.L. et al. (2020), Molecular Ecology Resources, 21, 849¿870, doi: 10.1111/1755-0998.13289; Keep, T. et al. (2021), Functional Ecology, 35, 1145¿1158, doi: 10.1111/1365-2435.13770; Keep, T. et al. (2021), Annals of Botany, 128, 357¿369, doi: 10.1093/aob/mcab057.20152017
Field trial of 385 natural populations and 12 cultivars of perennial ryegrass at Melle (ILVO) in Belgium (50.976 lat, 3.780 lon). The trial was sown on 2nd of October 2015. Each population or cultivar was sown in three 1m² micro-swards with 2g, 4g or 6g seeds according to whether its previously checked germination rate was higher than 80%, between 80 and 60%, or smaller than 60%, respectively. The populations and cultivars were sown in three complete blocks (replicates). The trial was monitored until end of 2017. Micro-swards were cut (all aerial biomass higher than 7 cm above ground surface) regularly as to simulate common cutting regime of meadows used for green forage production or grazing. Anti-dicotyledon herbicide was applied once in 2015 and a second time in 2016. A nitrogen fertilization was applied with 60 kg N ha-1 two months after sowing and after each aerial biomass cut and with 80 kg N ha-1 after winters 2015-2016 and 2016-2017 at start of spring growth. In this location, periods of moderate drought stress occurred during summer and autumn periods, notably during summer 2017 when soil water content fell below 27% of the soil water content at field capacity. The 12 cultivars used as controls were AberAvon, AberDart, Aurora, Barutti, Clerpin, Fennema, Lipresso, Mara, Meloni, Merks, Premium and Vigor.These C&E data were recorded in the frame of the project GrassLandscape (2015-2019) awarded by the FACCE-JPI ERA-NET+ call `Climate Smart Agriculture¿ (consortium: INRAE and EPHE in France, IPK in Germany, IBERS in the UK, ILVO in Belgium, project coordinator: JP Sampoux, INRAE). This project intended to discover climate adaptive genomic diversity in natural populations of perennial ryegrass and to relate adaptive loci to climate constraints and adaptive phenotypes. This project involved 385 natural populations of perennial ryegrass and 11 natural populations from related species originating from various regions of Europe and the Near-East. These populations were maintained as accessions in 15 genebanks of the ECPGR network and the USDA GRIN which provided seed samples. 14 perennial ryegrass cultivars were additionally used as checks. All accessions and cultivars were phenotyped for C&E data in three locations in Germany (IPK, Poel), Belgium(ILVO, Melle) and France (INRAE, Lusignan) from 2015 to 2017 or 2018 (according to location) and were genotyped for 507 583 SNP loci. The project identified 633 loci putatively involved in climate adaptation, among which 374 were positioned within or close to a gene. Papers published in the frame of the GrassLandscape project: Blanco-Pastor, J. L. et al. (2019), Journal of Biogeography (46), 1451-1465. , doi: 10.1111/jbi.13587; Keep, T. et al. (2020), Genes|Genomes|Genetics, doi:10.1534/g3.120.401491; Blanco-Pastor, J.L. et al. (2020), Molecular Ecology Resources, 21, 849¿870, doi: 10.1111/1755-0998.13289; Keep, T. et al. (2021), Functional Ecology, 35, 1145¿1158, doi: 10.1111/1365-2435.13770; Keep, T. et al. (2021), Annals of Botany, 128, 357¿369, doi: 10.1093/aob/mcab057.20152017
Field trial of 385 natural populations and 12 cultivars of perennial ryegrass at Lusignan (INRAE) in France (46.402 lat, 0.082 lon). The trial was sown on 9th of April 2015. Each population or cultivar was sown in three 1m² micro-swards with 2g, 4g or 6g seeds according to whether its previously checked germination rate was higher than 80%, between 80 and 60%, or smaller than 60%, respectively. The populations and cultivars were sown in three complete blocks (replicates). The trial was monitored until end of 2018. Micro-swards were cut (all aerial biomass higher than 7 cm above ground surface) regularly as to simulate common cutting regime of meadows used for green forage production or grazing. Anti-dicotyledon herbicide was applied once in 2015 in each location and a second time in 2016. A nitrogen fertilization was applied with 60 kg N ha-1 two months after sowing and after each aerial biomass cut and with 80 kg N ha-1 after winters 2015-2016 and 2016-2017 at start of spring growth. Drought stress was severe during summers 2016 and 2017 in this location with average soil water content falling below 20% of the soil water content at field capacity. The 12 cultivars used as controls were AberAvon, AberDart, Aurora, Barutti, Clerpin, Fennema, Lipresso, Mara, Meloni, Merks, Premium and Vigor.These C&E data were recorded in the frame of the project GrassLandscape (2015-2019) awarded by the FACCE-JPI ERA-NET+ call `Climate Smart Agriculture¿ (consortium: INRAE and EPHE in France, IPK in Germany, IBERS in the UK, ILVO in Belgium, project coordinator: JP Sampoux, INRAE). This project intended to discover climate adaptive genomic diversity in natural populations of perennial ryegrass and to relate adaptive loci to climate constraints and adaptive phenotypes. This project involved 385 natural populations of perennial ryegrass and 11 natural populations from related species originating from various regions of Europe and the Near-East. These populations were maintained as accessions in 15 genebanks of the ECPGR network and the USDA GRIN which provided seed samples. 14 perennial ryegrass cultivars were additionally used as checks. All accessions and cultivars were phenotyped for C&E data in three locations in Germany (IPK, Poel), Belgium(ILVO, Melle) and France (INRAE, Lusignan) from 2015 to 2017 or 2018 (according to location) and were genotyped for 507 583 SNP loci. The project identified 633 loci putatively involved in climate adaptation, among which 374 were positioned within or close to a gene. Papers published in the frame of the GrassLandscape project: Blanco-Pastor, J. L. et al. (2019), Journal of Biogeography (46), 1451-1465. , doi: 10.1111/jbi.13587; Keep, T. et al. (2020), Genes|Genomes|Genetics, doi:10.1534/g3.120.401491; Blanco-Pastor, J.L. et al. (2020), Molecular Ecology Resources, 21, 849¿870, doi: 10.1111/1755-0998.13289; Keep, T. et al. (2021), Functional Ecology, 35, 1145¿1158, doi: 10.1111/1365-2435.13770; Keep, T. et al. (2021), Annals of Botany, 128, 357¿369, doi: 10.1093/aob/mcab057.20152018
  • 1 - 3