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No description available.

No description available.

No description available.

No description available.

An evaluation of host-plant resistance to the wireworm-Diabrotica-Systena (WDS) complex of root-feeding insects in sweetpotatoes was performed on a total of 15 cultivars and advanced lines over the course of 4 years (2017-2020). It was found that sweetpotatoes varieties can differ significantly in amount of damage incurred. Several mechanisms of resistance were proposed and tested: periderm toughness, dry weight percentage, and volatile organic chemical defenses. No significant difference was found amongst the varieties tested concerning the physical properties. Chemical analysis was limited in scope but did show some differences between a susceptible variety when compared to a resistant variety in the volatile chemical composition of the foliage. Finally, a commercial kairomone lure with sticky card for Diabroticites was tested for efficacy when compared to sweep net sampling throughout the season. No correlation could be found amongst the methods in terms of number and species of insects caught by each.

Adaptive radiations provide exceptional opportunities to examine the relationships between natural selection, adaptation, and speciation. Neotropical Adelpha butterflies may represent such a radiation, characterized by extraordinary breadth in host plant use and wing color patterns. In this study, we use genome-wide RAD markers to reconstruct the complex evolutionary history of Adelpha and the closely related temperate genus, Limenitis. Despite the presence of significant missing data, a variety of phylogenetic methods produce similar and highly supported trees. These well-resolved phylogenies allow for the identification of an ecologically important shift to a toxic host plant family, as well as the confirmation of rampant wing pattern mimicry throughout the genus. Taken together, our results support the hypothesis that the colonization of novel host plants represents a key evolutionary innovation that is fueling ongoing adaptive diversification within this large, phenotypically diverse butterfly radiation.

Cotton (Gossypium hirsutum L.) crop maturity is delayed by cotton fleahopper (Pseudatomoscelis seriatus Reuter) (fleahopper) feeding on early-season fruit forms which increases vulnerability to late-season pests such as Helicoverpa zea (Boddie) and Heliothis virescens (Fabricius). The objectives of this research were to evaluate methods of screening for resistance to fleahopper and to screen selected genotypes. Six fleahoppers were caged on plants in the insectary for 72 h. Numbers of live fleahoppers and percent square damage were determined 48 h following the removal of fleahoppers. Fleahopper numbers and percent square set were determined on randomly selected plants of 16 genotypes when grown under field conditions in 2002 and 2003. Across multiple sampling dates, the number of fleahoppers per plant was higher (p=0.05) in G. arboreum and Pilose (G. hirsutum), but no consistent differences were observed among the remaining 15 genotypes which represented several germplasm pools across the United States. Field and no-choice feeding tests suggested that Pilose, Lankart 142, Suregrow 747, and Stoneville 474 were more resistant hairy-leaf genotypes and not different (p=0.05) in resistance than the smooth-leaf genotypes, Deltapine 50 and TAM 96WD-69s. Pin-head, match-head, and one-third grown squares were removed from plants and placed on agar in petri-plates. Four fleahoppers were released per plate and allowed to feed for 48 h. Fleahopper damage, brown areas along the anthers and/or brown and shrunken pollen sacs was most evident in pin-head sized squares.

On the Florida peninsula, the soapberry bug (Jadera haematoloma) has been able to colonize the golden rain tree, Koelreuteria elegans, since the introduction of this invasive tree only a few decades ago. The populations feeding on the new host have been rapidly differentiating from the native populations. Possibly the most dramatic differentiation is that of the beak (mouthpart) length. Derived populations showed shorter beaks more appropriate for feeding on the flattened pods of the new host. Previous studies have shown that the divergence of the beak length has a genetic basis and involves non-additive genetic effects. However, to date, the soapberry bug divergence has not been studied at the molecular level. In the current study, I have generated a three-generation pedigree from crossing the long-beaked and short-beaked ecomorphs to construct a de novo linkage map and to locate putative QTL controlling beak length and body size in J. haematoloma. Using the AFLP technique and a two-way pseudo-testcross design I produced two parental maps. The maternal map covered six linkage groups and the paternal map covered five; the expected number of chromosomes was recovered and the putative X chromosome was identified. For beak length, QTL analyses revealed one significant QTL. Three QTL were found for body size. Interestingly, the most significant body size QTL co-localized with the beak length QTL, suggesting linkage disequilibrium or pleiotropic effects of related traits. Through single marker regression analysis, nine single markers that could not be placed on the map were also found to be associated with either trait. However, I found no evidence for epistasis. Overall, my findings support an oligogenic model of genetic control on beak length and body size, and the underlying genetic architectures were complex. This study is the first to look at the molecular basis underlying adaptive traits in the soapberry bug, and contributes to understanding of the genetic changes involved in early stages of ecological divergence.

Cotton (Gossypium hirsutum L.) crop maturity is delayed by cotton fleahopper (Pseudatomoscelis seriatus Reuter) (fleahopper) feeding on early-season fruit forms which increases vulnerability to late-season pests such as Helicoverpa zea (Boddie) and Heliothis virescens (Fabricius). The objectives of this research were to evaluate methods of screening for resistance to fleahopper and to screen selected genotypes. Six fleahoppers were caged on plants in the insectary for 72 h. Numbers of live fleahoppers and percent square damage were determined 48 h following the removal of fleahoppers. Fleahopper numbers and percent square set were determined on randomly selected plants of 16 genotypes when grown under field conditions in 2002 and 2003. Across multiple sampling dates, the number of fleahoppers per plant was higher (p=0.05) in G. arboreum and Pilose (G. hirsutum), but no consistent differences were observed among the remaining 15 genotypes which represented several germplasm pools across the United States. Field and no-choice feeding tests suggested that Pilose, Lankart 142, Suregrow 747, and Stoneville 474 were more resistant hairy-leaf genotypes and not different (p=0.05) in resistance than the smooth-leaf genotypes, Deltapine 50 and TAM 96WD-69s. Pin-head, match-head, and one-third grown squares were removed from plants and placed on agar in petri-plates. Four fleahoppers were released per plate and allowed to feed for 48 h. Fleahopper damage, brown areas along the anthers and/or brown and shrunken pollen sacs was most evident in pin-head sized squares.