51 research outputs found
Flight with lift modulation inside a planetary atmosphere
Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/76287/1/AIAA-7461-486.pd
Time of flight secondary ion mass spectrometric determination of molecular weight distributions of low polydispersity poly(dimethyl siloxane) with polyatomic primary ions
Coding SNPs analysis highlights genetic relationships and evolution pattern in eggplant complexes
[EN] Brinjal (Solanum melongena), scarlet (S. aethiopicum) and gboma (S. macrocarpon) eggplants are three Old World domesticates. The genomic DNA of a collection of accessions belonging to the three cultivated species, along with a representation of various wild relatives, was characterized for the presence of single nucleotide polymorphisms (SNPs) using a genotype-by-sequencing approach. A total of 210 million useful reads were produced and were successfully aligned to the reference eggplant genome sequence. Out of the 75,399 polymorphic sites identified among the 76 entries in study, 12,859 were associated with coding sequence. A genetic relationships analysis, supported by the output of the FastSTRUCTURE software, identified four major sub-groups as present in the germplasm panel. The first of these clustered S. aethiopicum with its wild ancestor S. anguivi; the second, S. melongena, its wild progenitor S. insanum, and its relatives S. incanum, S. lichtensteinii and S. linneanum; the third, S. macrocarpon and its wild ancestor S. dasyphyllum; and the fourth, the New World species S. sisymbriifolium, S. torvum and S. elaeagnifolium. By applying a hierarchical FastSTRUCTURE analysis on partitioned data, it was also possible to resolve the ambiguous membership of the accessions of S. campylacanthum, S. violaceum, S. lidii, S. vespertilio and S. tomentsum, as well as to genetically differentiate the three species of New World Origin. A principal coordinates analysis performed both on the entire germplasm panel and also separately on the entries belonging to sub-groups revealed a clear separation among species, although not between each of the domesticates and their respective wild ancestors. There was no clear differentiation between either distinct cultivar groups or different geographical provenance. Adopting various approaches to analyze SNP variation provided support for interpretation of results. The genotyping-by-sequencing approach showed to be highly efficient for both quantifying genetic diversity and establishing genetic relationships among and within cultivated eggplants and their wild relatives. The relevance of these results to the evolution of eggplants, as well as to their genetic improvement, is discussed.This work has been funded in part by European Unions Horizon 2020 Research and Innovation Programme under grant agreement No 677379 (G2P-SOL project: Linking genetic resources, genomes and phenotypes of Solanaceous crops) and by Spanish Ministerio de Economia, Industria y Competitividad and Fondo Europeo de Desarrollo Regional (grant AGL2015-64755-R from MINECO/FEDER). Funding has also been received from the initiative "Adapting Agriculture to Climate Change: Collecting, Protecting and Preparing Crop Wild Relatives", which is supported by the Government of Norway. This last project is managed by the Global Crop Diversity Trust with the Millennium Seed Bank of the Royal Botanic Gardens, Kew and implemented in partnership with national and international gene banks and plant breeding institutes around the world. For further information see the project website:http://www.cwrdiversity.org/. Pietro Gramazio is grateful to Universitat Politecnica de Valencia for a pre-doctoral (Programa FPI de la UPV-Subprograma 1/2013 call) contract. Mariola Plazas is grateful to Spanish Ministerio de Economia, Industria y Competitividad for a post-doctoral grant within the Santiago Grisolia Programme (FCJI-2015-24835). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.Acquadro, A.; Barchi, L.; Gramazio, P.; Portis, E.; Vilanova Navarro, S.; Comino, C.; Plazas Ávila, MDLO.... (2017). Coding SNPs analysis highlights genetic relationships and evolution pattern in eggplant complexes. PLoS ONE. 12(7). https://doi.org/10.1371/journal.pone.0180774Se018077412
The effectiveness of growth cycles on improving fruit quality for grafted watermelon combinations
Mass selection for improvement of grain yield and protein in a maize population
Increasing grain protein concentration in maize (Zea mays L.) has not been a major focus of most breeding programs, which mainly focus on yield, maturity, and resistance to stress. The objective of this study was to evaluate the effectiveness of three cycles of mass selection to improve simultaneously yield and grain protein in the maize population GR-OP-319, derived from the F-2 generation of the single-cross hybrid PX-95. The two step selection procedure involved a stratified mass selection system that included check plants for environmental control. In the first step, plants having grain yield higher than 80% of the check-plant mean and protein concentration greater than the check-plant mean were selected. In the second step, the four plants within each selection grid having the highest protein concentration were selected, which resulted in a final selection intensity of 5%, Three cycles of selection were completed during 1991 to 1995. Response to selection was evaluated during the selection process and by direct field evaluation of the C-0, C-1, C-2, and C-3 populations in 1995 and 1996. The average response during the selection was 5.1% cycle(-1) for yield, 0.8 g kg(-1) cycle(-1) for protein concentration, and 7.0% cycle(-1) for protein yield. No measurable differences among cycles were observed in the direct field evaluation even though the trends in the means of the cycles followed the trends shown during selection. After three cycles, the mass selection system studied did not appear to be particularly effective
Determination of molecular weight and composition of a perfluorinated polymer from fragment intensities in time-of-flight secondary ion mass spectrometry
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