Application of mineral nutrients to improve plant health is critical to providing food and fiber. Potato (Solanum tuberosum L.) is among the most responsive species to N application but is susceptible to biotic and abiotic stresses. Nitrogen-stress relationships are generally evaluated indirectly during field fertility trials designed for collection of agronomic data. A controlled environment system would benefit understanding N nutrition-stress interactions. Environmental chamber hydroponics allows strict experimental control of temperature, humidity, light, etc. while maintaining specific N nutrition. Potatoes were grown at various N levels. Plant biomass had a curvilinear relationship with N supply, peaking at 80 mg N L⁻¹. Root or shoot N regressed against solution N produced significant, predictable relationships (R² > 0.98 for each). Such relationships provide a basis to conduct controlled N nutrition-abiotic-biotic stress studies that could delineate among stress factors. This work establishes the specific ranges of N needed to complete such research.

Background: Penstemon’s unique phenotypic diversity, hardiness, and drought-tolerance give it great potential for the xeric landscaping industry. Molecular markers will accelerate the breeding and domestication of drought tolerant Penstemon cultivars by, creating genetic maps, and clarifying of phylogenetic relationships. Our objectives were to identify and validate interspecific molecular markers from four diverse Penstemon species in order to gain specific insights into the Penstemon genome. Results: We used a 454 pyrosequencing and GR-RSC (genome reduction using restriction site conservation) to identify homologous loci across four Penstemon species (P. cyananthus, P. davidsonii, P. dissectus, and P. fruticosus) representing three diverse subgenera with considerable genome size variation. From these genomic data, we identified 133 unique interspecific markers containing SSRs and INDELs of which 51 produced viable PCR-based markers. These markers produced simple banding patterns in 90% of the species × marker interactions (~84% were polymorphic). Twelve of the markers were tested across 93, mostly xeric, Penstemon taxa (72 species), of which ~98% produced reproducible marker data. Additionally, we identified an average of one SNP per 2,890 bp per species and one per 97 bp between any two apparent homologous sequences from the four source species. We selected 192 homologous sequences, meeting stringent parameters, to create SNP markers. Of these, 75 demonstrated repeatable polymorphic marker functionality across the four sequence source species. Finally, sequence analysis indicated that repetitive elements were approximately 70% more prevalent in the P. cyananthus genome, the largest genome in the study, than in the smallest genome surveyed (P. dissectus). Conclusions: We demonstrated the utility of GR-RSC to identify homologous loci across related Penstemon taxa. Though PCR primer regions were conserved across a broadly sampled survey of Penstemon species (93 taxa), DNA sequence within these amplicons (12 SSR/INDEL markers) was highly diverse. With the continued decline in next-generation sequencing costs, it will soon be feasible to use genomic reduction techniques to simultaneously sequence thousands of homologous loci across dozens of Penstemon species. Such efforts will greatly facilitate our understanding of the phylogenetic structure within this important drought tolerant genus. In the interim, this study identified thousands of SNPs and over 50 SSRs/INDELs which should provide a foundation for future Penstemon phylogenetic studies and breeding efforts.

The Ascomycete fungus, Pyrenophora semeniperda, attacks a broad range of cool-season grasses. While leaf and predispersal infection of seeds (i.e., florets containing caryopses) have been previously characterized, little is known about the pathogenesis of mature seeds following dispersal. In this study, we examined infection and disease development of P. semeniperda on dormant seeds of Bromus tectorum. Inoculated seeds were hydrated at 20°C for up to 28 days. Disease development was characterized using scanning electron and light microscopy. P. semeniperda conidia germinated on the seed surface within 5 to 8 h. Hyphae grew on the seed surface and produced extracellular mucilage that eventually covered the seed. Appressoria formed on the ends of hyphae and penetrated through the lemma and palea, stomatal openings, and broken trichomes. The fungus then catabolized the endosperm, resulting in a visible cavity by 8 days. Pathogenesis of the embryo was associated with progressive loss of cell integrity and proliferation of mycelium. Beginning at approximately day 11, one to several stromata (approximately 150 μm in diameter and up to 4 mm in length) emerged through the lemma and palea. Degradation of embryo tissue was completed near 14 days. Conidiophores produced conidia between 21 and 28 days and often exhibited “Y-shaped” branching. This characterization of disease development corrects previous reports which concluded that P. semeniperda is only a weak seed pathogen with infection limited to the outermost seed tissues. In addition, the time required for disease development explains why infected dormant or slow-germinating seeds are most likely to experience mortality.

Many plant species exhibit strong seed dormancy. This attribute benefits the species’ long-term survival but can impede restoration when rapid establishment is required. Soaking seeds in gibberellic acid (GA₃) can overcome dormancy and increase germination but this treatment may not be effective outside the laboratory. An easier and potentially more effective method to apply this hormone is to coat seeds with a GA₃-impregnated polymer. Seed dormancy can also be mitigated by creating a favorable microsite with increased soil moisture. We compared the emergence and establishment of penstemon seeds coated with GA₃ to those of uncoated seeds planted in shallow drill rows versus deep, U-shaped furrows. Overall, 6 times more Palmer’s penstemon (Penstemon palmeri; p < 0.01) and 21 times more thickleaf penstemon (P. pachyphyllus; p < 0.001) established when coated with GA₃, but GA₃ coating did not affect the establishment of firecracker penstemon (P. eatonii; p = 1). Establishment was higher from deep furrows than shallow rows (p < 0.001). These results indicate that GA₃ seed coating and deep, U-shaped furrows may improve the restoration success of some native forbs by breaking dormancy and providing a favorable microsite. Land managers could use these techniques to restore native forbs in dry, disturbed areas.