Konza LTER Publications
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Phytobiome stampede: Bison as potential dispersal agents for the tallgrass prairie microbiome. PhytoFrontiers™. In Press. doi:10.1094/PHYTOFR-01-23-0004-SC.
. Plant responses to changing rainfall frequency and magnitude. Nature Ecology & Evolution. In Press.
Product-inhibition feedbacks, not microbial population level tradeoffs or soil pH, regulate decomposition potential under nutrient eutrophication. Soil Biology and Biochemistry. 2024;189:109247. doi:10.1016/j.soilbio.2023.109247.
. Persistent decadal differences in plant communities assembled under contrasting climate conditions. Ecological Applications. 2023;33(2):e2823. doi:10.1002/eap.2823.
. Prairie plant communities and their associated phyllosphere fungal communities change across the steep precipitation gradient in Kansas USA, though individual plant species’ phyllosphere communities may not. Department of Biology. 2023;MS Thesis. Available at: https://krex.k-state.edu/bitstream/handle/2097/43453/HannahDea2023.pdf?sequence=12.
. Partitioning evapotranspiration in a tallgrass prairie using micrometeorological and water use efficiency approaches under contrasting rainfall regimes. Journal of Hydrology. 2022;608:127624. doi:10.1016/j.jhydrol.2022.127624.
. Poor relationships between NEON Airborne Observation Platform data and field‐based vegetation traits at a mesic grassland. Ecology. 2022;103(2):e03590. doi:10.1002/ecy.v103.210.1002/ecy.3590.
Post-silking 15N labelling reveals an enhanced nitrogen allocation to leaves in modern maize (Zea mays) genotypes. Journal of Plant Physiology. 2022;268:153577. doi:10.1016/j.jplph.2021.153577.
. Prairie stream metabolism recovery varies based on antecedent hydrology across a stream network after a bank‐full flood. Limnology and Oceanography. 2022;67(9):1986-1999. doi:10.1002/lno.12182.
. Precipitation effects on nematode diversity and carbon footprint across grasslands. Global Change Biology. 2022;28(6):2124-2132. doi:10.1111/gcb.16055.
Precipitation, not land use, primarily determines the composition of both plant and phyllosphere fungal communities. Frontiers in Fungal Biology. 2022;3:805225. doi:10.3389/ffunb.2022.805225.
Predation, parasitism, and drought counteract the benefits of patch-burn grazing for the reproductive success of grassland songbirds. Ornithological Applications. 2022;124:1–22. doi:10.1093/ornithapp/duab066.
Patterns and trends of organic matter processing and transport: Insights from the US Long-Term Ecological Research network. Climate Change Ecology. 2021;2:100025. doi:10.1016/j.ecochg.2021.100025.
Plant diversity and litter accumulation mediate the loss of foliar endophyte fungal richness following nutrient addition. Ecology. 2021;102(1):e03210. doi:10.1002/ecy.3210.
. Plant legacies and soil microbial community dynamics control soil respiration. Soil Biology and Biochemistry. 2021;160:108350. doi:10.1016/j.soilbio.2021.108350.
. Precipitation manipulation and terrestrial carbon cycling: The roles of treatment magnitude, experimental duration and local climate. . Global Ecology and Biogeography. 2021;30(9):1909 - 1921. doi:10.1111/geb.13356.
Precipitation–productivity relationships and the duration of precipitation anomalies: An underappreciated dimension of climate change. Global Change Biology. 2021;27(6):1127 - 1140. doi:10.1111/gcb.15480.
. Is a prescribed fire sufficient to slow the spread of woody plants in an infrequently burned grassland? A case study in tallgrass prairie. Rangeland Ecology & Management. 2021;78:79 - 89. doi:10.1016/j.rama.2021.05.007.
. Plant phylogenetic history explains in‐stream decomposition at a global scale. . Journal of Ecology. 2020;108(1):17-35. doi:10.1111/1365-2745.13262.
Plant–microbial interactions facilitate grassland species coexistence at the community level. Oikos. 2020;129(4):533-543. doi:10.1111/oik.06609.
Populations of small mammals, tallgrass prairie and prescribed fire: A fire-reversal experiment. Transactions of the Kansas Academy of Science. 2020;123(1-2):1. doi:10.1660/062.123.0101.
. Precipitation amount and event size interact to reduce ecosystem functioning during dry years in a mesic grassland. Global Change Biology. 2020;26(2):658-668. doi:10.1111/gcb.14789.
. Periodical cicada emergence resource pulse tracks forest expansion in a tallgrass prairie landscape. Ecosphere. 2019;10(7):e02779. 10.1002/ecs2.2779. doi:10.1002/ecs2.2019.10.issue-710.1002/ecs2.2779.
Phenology-adjusted dynamic curve number for improved hydrologic modeling. Journal of Environmental Management. 2019;235:403 - 413. doi:10.1016/j.jenvman.2018.12.115.
. Phosphorus and mowing improve native alfalfa establishment, facilitating restoration of grassland productivity and diversity. Land Degradation & Development. 2019;30(6):647 - 657. doi:10.1002/ldr.v30.610.1002/ldr.3251.
. A practical guide for combining data to model species distributions. Ecology. 2019;81:e02710. doi:10.1002/ecy.2710.
. Partitioning assimilatory nitrogen uptake in streams: an analysis of stable isotope tracer additions across continents. Ecological Monographs. 2018;88(1):138. doi:10.1002/ecm.1280.
Patterns and correlates of within-season breeding dispersal: a common strategy in a declining grassland songbird. The Auk: Ornithological Advances. 2018;135(1):1-14. doi:10.1642/AUK-17-69.1.
. Physiological and anatomical trait variability of dominant C4 grasses. Acta Oecologica. 2018;93:14 - 20. doi:10.1016/j.actao.2018.10.007.
. Plant functional group influences arbuscular mycorrhizal fungal abundance and hyphal contribution to soil CO2 efflux in temperate grasslands. Plant and Soil. 2018;432(1-1):157-170. doi:10.1007/s11104-018-3789-0.
Partitioning the CO2 net flux into assimilation and respiration components, and estimating water use efficiency in a grassland ecosystem. 2017;MS Thesis.
. Phenotypic distribution models corroborate species distribution models: A shift in the role and prevalence of a dominant prairie grass in response to climate change. Global Change Biology. 2017;23(10):4365–4375. doi:10.1111/gcb.13666.
. Photosynthetic responses of a dominant C4 grass to an experimental heat wave are mediated by soil moisture. Oecologia. 2017;183(1):303-313. doi:10.1007/s00442-016-3755-6.
. Physiological and morphological responses of grass species to drought. Department of Biology. 2017;MS Thesis. Available at: http://krex.k-state.edu/dspace/handle/2097/36188.
. Precipitation and environmental constraints on three aspects of flowering in three dominant tallgrass species. Functional Ecology. 2017. doi:10.1111/1365-2435.12904.
. Probing whole-stream metabolism: influence of spatial heterogeneity on rate estimates. Freshwater Biology. 2017;62(4):711 - 723. doi:10.1111/fwb.12896.
. Prospective evidence for independent nitrogen and phosphorus limitation of grasshopper (Chorthippus curtipennis) growth in a tallgrass prairie. PLoS One. 2017;12(5):e0177754. doi:10.1371/journal.pone.0177754.
. Pushing precipitation to the extremes in distributed experiments: recommendations for simulating wet and dry years. Global Change Biology. 2017;23(5):1774-1782. doi:10.1111/gcb.13504.
Patch-burn grazing increases habitat heterogeneity and biodiversity of small mammals in managed rangelands. Ecosphere. 2016;7(8):e01431. doi:10.1002/ecs2.1431.
. Patterns and ecological consequences of water uptake, redistribution, and loss in tallgrass prairie. 2016;PhD Dissertation. Available at: http://krex.k-state.edu/dspace/handle/2097/34514.
. Productivity of North American grasslands is increased under future climate scenarios despite rising aridity. Nature Climate Change. 2016;6:710-714. doi:10.1038/nclimate2942.
Patch-burn grazing effects on the ecological integrity of tallgrass prairie streams. Journal of Environment Quality. 2015;44(4):1148. doi:10.2134/jeq2014.10.0437.
. Plant diversity predicts beta but not alpha diversity of soil microbes across grasslands worldwide. Ecology Letters. 2015;18:85 -95. doi:10.1111/ele.12381.
Plant responses to grazer-mediated habitat alterations in tallgrass prairie. 2015;MS Thesis. Available at: http://krex.k-state.edu/dspace/handle/2097/19065.
. Plant species’ origin predicts dominance and response to nutrient enrichment and herbivores in global grasslands. Nature Communications. 2015;6:7710 -. doi:10.1038/ncomms8710.
Plains harvest mice in tallgrass prairie: abundance, habitat association and individual attributes. Transactions of the Kansas Academy of Science. 2014;117:167 -180. doi:10.1660/062.117.0302.
. Plant community response to loss of large herbivores differs between North American and South African savanna grasslands. Ecology. 2014;95:808 -816. doi:10.1890/13-1828.1.
Plant-virus interactions and the agro-ecological interface. European Journal of Plant Pathology. 2014;138:529 -537. doi:10.1007/s10658-013-0317-1.
. Patterns of diversity and adaptation in Glomeromycota from three prairie grasslands. Molecular Ecology. 2013;22:2573 -2587. doi:10.1111/mec.12268.
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