Konza LTER Publications
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Nutrients cause grassland biomass to outpace herbivory. Nature Communications. 2020;11(1):6036. doi:10.1038/s41467-020-19870-y.
Nutrients cause grassland biomass to outpace herbivory. Nature Communications. 2020;11(1):6036. doi:10.1038/s41467-020-19870-y.
Observations and modeling of biomass and soil organic matter dynamics for the grassland biome worldwide. Global Biogeochemical Cycles. 1993;7:785 -809. doi:10.1029/93GB02042.
Observations and modeling of biomass and soil organic matter dynamics for the grassland biome worldwide. Global Biogeochemical Cycles. 1993;7:785 -809. doi:10.1029/93GB02042.
Observations and modeling of biomass and soil organic matter dynamics for the grassland biome worldwide. Global Biogeochemical Cycles. 1993;7:785 -809. doi:10.1029/93GB02042.
Observations and modeling of biomass and soil organic matter dynamics for the grassland biome worldwide. Global Biogeochemical Cycles. 1993;7:785 -809. doi:10.1029/93GB02042.
Observing spatial structure in the Flint Hills using AVHRR biweekly composites of maximum NDVI. . 1995:143 -151.
. Odor as a factor in nut discovery by fox squirrels. Transactions of the Kansas Academy of Science. 1994;97:1 -3. doi:10.2307/3628246.
. Of mice and coyotes: mammalian responses to rangeland management practices in tallgrass prairie. 2016;PhD Dissertation. Available at: http://krex.k-state.edu/dspace/handle/2097/32731.
. Optimal staining and sample storage time for direct microscopic enumeration of total and active bacteria in soil with two fluorescent dyes. Applied and Environmental Microbiology. 1995;61:3367 -3372. Available at: http://aem.asm.org/content/61/9/3367.short.
. Optimal staining and sample storage time for direct microscopic enumeration of total and active bacteria in soil with two fluorescent dyes. Applied and Environmental Microbiology. 1995;61:3367 -3372. Available at: http://aem.asm.org/content/61/9/3367.short.
. Optimizing radio retention andminimizing radio impacts in a field study of Upland Sandpipers. Journal ofWildlife Management. 2007;71:971 -980. doi:10.2193/2005-775.
. Organic matter loading and processing in a pristine stream draining a tallgrass prairie/riparian forest watershed. Kansas Water Resources Research Institute Contribution No. 1982;230:1 -78.
. Out of the shadows: multiple nutrient limitations drive relationships among biomass, light and plant diversity. . Functional Ecology. 2017;31(9):1839-1846. doi:10.1111/1365-2435.12967.
Out of the shadows: multiple nutrient limitations drive relationships among biomass, light and plant diversity. . Functional Ecology. 2017;31(9):1839-1846. doi:10.1111/1365-2435.12967.
Out of the shadows: multiple nutrient limitations drive relationships among biomass, light and plant diversity. . Functional Ecology. 2017;31(9):1839-1846. doi:10.1111/1365-2435.12967.
Out of the shadows: multiple nutrient limitations drive relationships among biomass, light and plant diversity. . Functional Ecology. 2017;31(9):1839-1846. doi:10.1111/1365-2435.12967.
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.
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.
. Partitioning of dissolved inorganic or organic phosphorus using acidified molybdate and isobutanol. Soil Science Society of American Journal. 1992;56:762 -765. doi:10.2136/sssaj1992.03615995005600030014x.
. Past, present, and future roles of long-term experiments in the LTER Network. Bioscience. 2012;62:377 -389. doi:10.1525/bio.2012.62.4.9.
Past, present, and future roles of long-term experiments in the LTER Network. Bioscience. 2012;62:377 -389. doi:10.1525/bio.2012.62.4.9.
Past, present, and future roles of long-term experiments in the LTER Network. Bioscience. 2012;62:377 -389. doi:10.1525/bio.2012.62.4.9.
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 of macroinvertebrate production, trophic structure, and energy flow along a tallgrass prairie stream continuum. Limnology and Oceanography. 2011;56:887 -898. doi:10.4319/lo.2011.56.3.0887.
. Patterns of trait convergence and divergence among native and exotic species in herbaceous plant communities are not modified by nitrogen enrichment. Journal of Ecology. 2011;99:1327 -1338. doi:10.1111/j.1365-2745.2011.01860.x.
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.
Persistent decadal differences in plant communities assembled under contrasting climate conditions. Ecological Applications. 2023;33(2):e2823. doi:10.1002/eap.2823.
. Phenological influences on the albedo of prairie grassland and crop fields. International Journal of Biometeorology. 1999;42:153 -157. doi:10.1007/s004840050099.
. Phenologies of North American Grasslands and Grasses. In: Phenology: An Integrative Environmental Science, 2e. Phenology: An Integrative Environmental Science, 2e. Springer Netherlands; 2013:197-210. doi:10.1007/978-94-007-6925-0_11.
. Phenotypic correlates and survival consequences of male mating success in lek-mating Greater Prairie-chickens (Tympanuchus cupido). Behavioral Ecology and Sociobiology. 2008;62:1377 -1388. doi:10.1007/s00265-008-0566-8.
. 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 traits of exotic, invasive exotic, and native plant species in tallgrass prairie. International Journal of Plant Sciences. 2001;162:785 -792. doi:10.1086/320774.
. Physiological interactions along resource gradients in a tallgrass prairie. Ecology. 1991;72:672 -684. doi:10.2307/2937207.
. Physiological interactions along resource gradients in a tallgrass prairie. Ecology. 1991;72:672 -684. doi:10.2307/2937207.
. Phytobiome stampede: Bison as potential dispersal agents for the tallgrass prairie microbiome. PhytoFrontiers™. In Press. doi:10.1094/PHYTOFR-01-23-0004-SC.
. Plant and soil responses to high and low diversity grassland restoration practices. Environmental Management. 2012;49:412 -424. doi:10.1007/s00267-011-9787-0.
. 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 demographic responses to mycorrhizal symbiosis in tallgrass prairie. Oecologia. 1994;99:21 -26. doi:10.1007/BF00317079.
. 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 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 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 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 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.
Plant pathogens as indicators of climate change. In: Climate and Global Change: Observed Impacts on Planet Earth. Climate and Global Change: Observed Impacts on Planet Earth. Elsevier; 2009:425 -437. Available at: http://pdf.usaid.gov/pdf_docs/PNADU515.pdf.
. 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 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 species’ origin predicts dominance and response to nutrient enrichment and herbivores in global grasslands. Nature Communications. 2015;6:7710 -. doi:10.1038/ncomms8710.
Plasma cholinesterases for monitoring pesticide exposure in Nearctic-Neotropical migratory shorebirds. Ornithología Neotropical. 2008;19 (Suppl):641 -651. Available at: https://www.researchgate.net/publication/254414753_Plasma_cholinesterases_for_monitoring_pesticide_exposure_in_Nearctic-Neotropical_migratory_shorebirds.