Tolerance of peppermint to tiafenacil applied postharvest

Trials were conducted in two experimental runs at the Purdue University Horticulture Greenhouses, West Lafayette, IN, to determine ‘Redefined Murray Mitcham’ peppermint tolerance to tiafenacil. Established peppermint in 20-cm-diameter polyethylene pots was subjected to a simulated harvest by removing aboveground biomass at the substrate surface; then, tiafenacil was applied at 0, 25, 50, 100, and 200 g ai ha−1. Visible crop injury, height, and aboveground dry biomass data were subjected to regression analysis to generate predictive models. At 2 wk after treatment (WAT), peppermint injury increased from 63% to 86% and from 25% to 76% in Experimental Run 1 and 2, respectively, as tiafenacil rate increased from 25 to 200 g ha−1. At 4 WAT, injury increased from 0% to 63% and from 4% to 37% in Experimental Run 1 and 2, respectively, as tiafenacil rate increased from 25 to 200 g ha−1. By 7 WAT (both experimental runs), injury increased from 0% to 17% as tiafenacil rate increased from 25 to 200 g ha−1. At 4 WAT, height decreased from 23.0 to 8.6 cm and from 17.6 to 10.3 cm in Experimental Run 1 and 2, respectively, as tiafenacil rate increased from 0 to 200 g ha−1. At 7 WAT, height decreased from 28.1 to 21.4 cm as tiafenacil rate increased from 0 to 200 g ha−1. Aboveground dry weight of the nontreated check was 20.3 g pot−1 and decreased from 19.3 to 7.0 g pot−1 as tiafenacil rate increased from 25 to 200 g ha−1. Despite acute necrosis, injury from tiafenacil at lower rates was not persistent. The proposed 1X rate of tiafenacil for peppermint, 25 g ha−1, resulted in ≤4% injury 4 and 7 WAT and in only a 3% reduction in plant height and a 4.7% reduction in aboveground dry weight compared to the nontreated check

Internships: The Nuts And Bolts Of An Effective Program

Braxston Public Engineering and Consulting Group (BPECG) is a nationally known and respected company that is magnate for students who wish to receive a valued internship experience.   Under the able direction of Amy Greene, the work experiences were coordinated during the summer and interns were well paid for their contributions.  The case study chronicles the trials and tribulations faced by a competent, highly energized engineering intern who faces the malaise of an organization that is unprepared to provide a valid learning experience. As the case unfolds, Greene has an Eureka experience and learns from a colleague how interns can and do make vital contributions (ROI’s) to their assigned organizations. Upon reviewing the contributions that interns made in three organizations, she redesigns Braxston’s Internship program, reviews the State University Intern to Work Program that addresses, among many other factors, the internship purpose, supervision, learning objectives,  and intern and employer obligations.  The case includes an Intern Evaluation form and a Memorandum of Understanding (MOU) between the university and the company. Last, the Questions and Instructions provide for focused discussion and analysis and the references enable learners to research the top internship programs in the United States

Dicamba residue persistence in processing tomato

There is zero tolerance for dicamba and dicamba metabolite residue in tomato (Solanum lycopersicum L.) fruit following exposure to dicamba. Field trials were conducted in 2020 and 2021 to determine the persistence of dicamba and metabolite (5-hydroxy dicamba and 3,6-dichlorosalicylic acid [DCSA]) residue in processing tomato shoots and fruits. Dicamba was applied 49 d after transplanting at 0, 0.53, 5.3, and 53 g ae ha−1. Tomato plants were harvested 5, 10, 20, 40, and 61 d after treatment (DAT). No 5-hydroxy dicamba was recovered from any sample. In 2020, the DCSA metabolite was detected from tomato shoot tissue when dicamba was applied at the 53 g ha−1 rate at 0 (14 µg kg−1), 5 (3 µg kg−1), and 20 DAT (5 µg kg−1) and from tomato fruit tissue at 53 g ha−1 at 20 (2 µg kg−1) and 61 DAT (2 µg kg−1). In 2021, DCSA was not detected from tomato shoot or fruit tissues at any harvest date. By 5 DAT, dicamba was only detected from tomato shoot tissues treated with 53 g ha−1. At 0 DAT, dicamba residue was detectable only from tomato fruit on plants treated with 53 g ha−1. Tomato fruit dicamba residue from plants treated with 5.3 g ha−1 had a predicted peak of 19 µg kg−1 at 11.3 DAT. Tomato fruit dicamba residue from plants treated with 53 g ha−1 decreased from 164 to 8 µg kg−1 from 5 to 61 DAT. Furthermore, this study confirms that dicamba is detectable from tomato fruits at 61 DAT following exposure to 5.3 or 53 g ha−1 dicamba. Growers who suspect dicamba exposure should include tomato fruit tissue with their collected sample or sample tomato fruits separately

An Evaluation of Putative Sympatric Speciation within Limnanthes (Limnanthaceae)

Limnanthes floccosa ssp. floccosa and L. floccosa ssp. grandiflora are two of five subspecies within Limnanthes floccosa endemic to vernal pools in southern Oregon and northern California. Three seasons of monitoring natural populations have quantified that L. floccosa ssp. grandiflora is always found growing sympatrically with L. floccosa ssp. floccosa and that their flowering times overlap considerably. Despite their subspecific rank within the same species crossing experiments have confirmed that their F1 hybrids are sterile. An analysis of twelve microsatellite markers, with unique alleles in each taxon, also shows exceedingly low levels of gene flow between populations of the two subspecies. Due to the lack of previous phylogenetic resolution among L. floccosa subspecies, we used Illumina next generation sequencing to identify single nucleotide polymorphisms from genomic DNA libraries of L. floccosa ssp. floccosa and L. floccosa ssp. grandiflora. These data were used to identify single nucleotide polymorphisms in the chloroplast, mitochondrial, and nuclear genomes. From these variable loci, a total of 2772 bp was obtained using Sanger sequencing of ten individuals representing all subspecies of L. floccosa and an outgroup. The resulting phylogenetic reconstruction was fully resolved. Our results indicate that although L. floccosa ssp. floccosa and L. floccosa ssp. grandiflora are closely related, they are not sister taxa and therefore likely did not diverge as a result of a sympatric speciation event

Taxonomic Clarification of Lupinus oreganus and Lupinus biddlei in the Pacific Northwest, USA

Through a phylogenetic study Using LECCYCIA nucleotide sequences and a survey of historical Botanical literature, we propose clarifications in the nomenclature of Lupinus oreganus and Lupinus biddlei. The former taxon has been incorrectly classified as Lupinus sulphurcus ssp. kincaidii and recently as L. oreganus var. kincaidii. The latter has recently been incorrectly delimited as L. oreganus var. oreganus.This is the publisher’s final pdf. The published article is copyrighted by Western North American Naturalist Publications and can be found at: https://ojs.lib.byu.edu/wnan/.Keywords: Genes, Leguminosa

Ethofumesate-resistant annual bluegrass (Poa annua) in grass seed production systems

The prolific seed production and polyploidy of annual bluegrass allow for the rapid development of herbicide resistance. Ethofumesate-resistant annual bluegrass plants were identified in the 1990s in grass seed production in Oregon, but their prevalence and distribution are not well documented. Therefore a dose–response experiment was initiated to determine the potential level of ethofumesate resistance in seed production systems. Seeds from 55 annual bluegrass populations were obtained from three sources: seed production fields (31 populations), the seed cleaning process (6 populations), and seed testing lots prior to retail distribution (18 populations). Additionally, two populations, one with known ethofumesate resistance and one with known susceptibility, were identified in preliminary testing and used as controls in this experiment. Seed from each collected population was increased. Individual seedlings were then transplanted into separate cone-tainers, grown to a size of 2 to 3 tillers in the greenhouse, and then sprayed using a compressed air track spray chamber with 10 doses of ethofumesate at 0, 0.56, 1.1, 2.8, 5.6, 8.4, 11.2, 16.8, 22.4, and 44.8 kg ai ha−1, with 0.84 to 2.2 kg ha−1 as the label application rate for perennial ryegrass. The resistant to susceptible ratio of populations across all sources ranged from 0.5 to 5.5. The most resistant populations found in production fields, seed cleaning, and seed testing lots had the effective dose necessary to kill 50% of the population (ED50) of 12.1, 9.4, and 13.1 kg ha−1, respectively. Furthermore, 68% of the populations found in production fields had ED50 higher than 6 kg ha−1, indicating common annual bluegrass resistance in grass seed production. As such, growers should implement integrated weed management strategies, as herbicides alone will likely be ineffective at controlling annual bluegrass

Connective tissue activation. XVII. Radioimmunoassay of a human platelet derived connective tissue activating peptide (CTAP-III) and specificities of anti-CTAP-III sera

The platelet-derived connective tissue activating peptide (CTAP-III) has been shown to be an important factor stimulating the metabolism and proliferation of human connective tissue cell strains, including synovial tissue cells. The quantities of CTAP-III affecting the cellular changes and the amounts in various biologic fluids and tissues are small. The objectives of this study were to develop a radioimmunoassay (RIA) for CTAP-III and to ascertain the specificities of the anti-CTAP-III sera reagents. The antisera were shown not to cross-react with a number of polypeptide hormones. However, two other platelet proteins, [beta]-thromboglobulin and low affinity platelet factor-4, competed equally as well as CTAP-III for anti-CTAP-III antibodies in the RIA system. Thus, the three platelet proteins are similar or identical with respect to those portions of the molecules constituting the reactive antigenic determinants. The levels of material in normal human platelet-free plasma that inhibited anti-CTAP-III-12S!-CTAP-III complex formation were determined to be 34 +/- 13 (S.D.) ng/ml.Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/23085/1/0000002.pd

An Evaluation of Putative Sympatric Speciation within Limnanthes (Limnanthaceae)

Limnanthes floccosa ssp. floccosa and L. floccosa ssp. grandiflora are two of five subspecies within Limnanthes floccosa endemic to vernal pools in southern Oregon and northern California. Three seasons of monitoring natural populations have quantified that L. floccosa ssp. grandiflora is always found growing sympatrically with L. floccosa ssp. floccosa and that their flowering times overlap considerably. Despite their subspecific rank within the same species crossing experiments have confirmed that their F1 hybrids are sterile. An analysis of twelve microsatellite markers, with unique alleles in each taxon, also shows exceedingly low levels of gene flow between populations of the two subspecies. Due to the lack of previous phylogenetic resolution among L. floccosa subspecies, we used Illumina next generation sequencing to identify single nucleotide polymorphisms from genomic DNA libraries of L. floccosa ssp. floccosa and L. floccosa ssp. grandiflora. These data were used to identify single nucleotide polymorphisms in the chloroplast, mitochondrial, and nuclear genomes. From these variable loci, a total of 2772 bp was obtained using Sanger sequencing of ten individuals representing all subspecies of L. floccosa and an outgroup. The resulting phylogenetic reconstruction was fully resolved. Our results indicate that although L. floccosa ssp. floccosa and L. floccosa ssp. grandiflora are closely related, they are not sister taxa and therefore likely did not diverge as a result of a sympatric speciation event

Genomic and small RNA sequencing of Miscanthus × giganteus shows the utility of sorghum as a reference genome sequence for Andropogoneae grasses

Genomic data together with sequencing of tissue specific small RNA libraries reveals insights into the genome content, small RNA repertoire and evolutionary origins of the grass Miscanthus × giganteus