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Data from: Phenotypic and nodule microbial diversity among crimson clover (Trifolium incarnatum L.) accessions

    Phenotypic evaluation of 37 crimson clover (Trifolium incarnatum L.) accessions from the US National Plant Germplasm System. Focus of the trial was on traits important for cover crop performance, including fall emergence, winter survival, flowering time, biomass, nitrogen (N) content in aboveground biomass, and proportion of plant N from biological nitrogen fixation (BNF). Experiments were conducted at the Beltsville Agricultural Research Center (Maryland, USA) across three growing seasons (2012-2013, 2013-2014, 2014-2015).

    Kellogg Soil Survey Laboratory (KSSL) POX-C dataset

      Forty two samples were selected from the Kellogg Soil Survey Laboratory (KSSL) archive. The soils (41) were taken from the A horizon except for one sample that came from an O horizon. The samples represented 9 of the 12 US soil Orders, including Mollisols (23), Alfisols (5), Ultisols (5), Andisols (2), Entisols (2), Inceptisols (2), Aridisols (1), Histosols (1) and Vertisols (1). The soils varied widely in SOC (3.0 – 288.4 g kg-1; mean 31 g kg-1), pH (4.3 – 8.5; mean 6.2) and clay content (3.6 – 47.0%; mean 21.5%) The geographic origin of the selected samples and the distribution of SOC concentrations, clay contents and pH values are in the sample selected materials.

      Data from: Pyrosequencing-Based Analysis of the Microbiome Associated with the Horn Fly, Haematobia irritans

        The bacterial 16S tag-encoded FLX-titanium amplicon pyrosequencing (bTEFAP) method was used to carry out the classification analysis of bacterial flora in adult female and male horn flies and horn fly eggs. The bTEFAP method identified 16S rDNA sequences in our samples which allowed the identification of various prokaryotic taxa associated with the life stage examined. This is the first comprehensive report of bacterial flora associated with the horn fly using a culture-independent method. Several rumen, environmental, symbiotic and pathogenic bacteria associated with the horn fly were identified and quantified. This is the first report of the presence of Wolbachia in horn flies of USA origin and is the first report of the presence of Rikenella in an obligatory blood feeding insect.