Konza LTER Publications
] . Interacting influence of mycorrhizal symbiosis and competition on plant diversity in tallgrass prairie. Oecologia. 1999;121:574 -582. doi:10.1007/s004420050964.
. Invasibility of a mesic grassland depends on the time-scale of fluctuating resources. Journal of Ecology. 2015;103(6):1538 - 1546. doi:10.1111/1365-2745.12479.
Invasion in space and time: non-native species richness and relative abundance respond to interannual variation in productivity and diversity. Ecology Letters. 2004;7:947 -957. doi:10.1111/j.1461-0248.2004.00655.x.
. Invasion of an intact plant community: the role of population vs. community level diversity. Oecologia. 2012;168:1091 -1102. doi:10.1007/s00442-011-2157-z.
. Invertebrate, not small vertebrate, herbivory interacts with nutrient availability to impact tallgrass prairie community composition and forb biomass. Oikos. 2015;124:842 -850. doi:10.1111/oik.01869.
Loss of a large grazer impacts savanna grassland plant communities similarly in North America and South Africa. Oecologia. 2014;175:293 -303. doi:10.1007/s00442-014-2895-9.
. Measuring genetic diversity in ecological studies. Plant Ecology. 2012;213:1105 -1115. doi:10.1007/s11258-012-0069-6.
. Mechanisms of selection: Phenotypic differences among genotypes explain patterns of selection in a dominant species. Ecology. 2013;94:953 -965. doi:10.1890/12-1119.1.
. Nutrient additions cause divergence of tallgrass prairie plant communities resulting in loss of ecosystem stability. Journal of Ecology. 2016;104:1478-1487. doi:10.1111/1365-2745.12610.
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.
. 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.
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.
. Precipitation and environmental constraints on three aspects of flowering in three dominant tallgrass species. Functional Ecology. 2017. doi:10.1111/1365-2435.12904.
Predicting invasion in grassland ecosystems: is exotic dominance the real embarrassment of richness?. Global Change Biology. 2013;19(12):3677 - 3687. doi:10.1111/gcb.12370.
. Prospective evidence for independent nitrogen and phosphorus limitation of grasshopper (Chorthippus curtipennis) growth in a tallgrass prairie. PLoS One. 2017. 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.
Rainfall variability, carbon cycling and plant species diversity in a mesic grassland. Science. 2002;298:2202 -2205. doi:10.1126/science.1076347.
. Rainfall variability has minimal effects on grassland recovery from repeated grazing. Journal of Vegetation Science. 2014;25:36 -44. doi:10.1111/jvs.12065.
. Rangeland responses to predicted increases in drought extremity. Rangelands . 2016;38:191-196. Available at: http://dx.doi.org/10.1016/j.rala.2016.06.009.
. Reconciling inconsistencies in precipitation– productivity relationships: implications for climate change. New Phytologist. 2017;214(1):41-47. doi:10.1111/nph.14381.
. Relative effects of precipitation variability and warming on tallgrass prairie ecosystem function. Biogeosciences. 2011;8:3053 -3068. doi:10.5194/bg-8-3053-2011.
. Resistance and resilience of a grassland ecosystem to climate extremes. Ecology. 2014;95:2646 -2656. doi:10.1890/13-2186.1.
. Resource availability modulates above and belowground competitive interactions between genotypes of a dominant C4 grass. Functional Ecology. 2014;28:1041 -1051. doi:10.1111/1365-2435.12227.
Responses to fire differ between South African and North American grassland communities. Journal of Vegetation Science. 2014;25:793 -804. doi:10.1111/jvs.12130.
. Scale dependence in the relationship between species richness and productivity: the role of spatial and temporal turnover. Ecology. 2004;85:2701 -2708. doi:10.1890/03-0561.
. Scale-dependent interaction of fire andgrazing on community heterogeneity in tallgrass prairie. Ecology. 2006;87:2058 -2067. doi:10.1890/0012-9658(2006)87[2058:SIOFAG]2.0.CO;2.
Shared drivers but divergent ecological responses: Insights from long-term experiments in mesic savanna grasslands. BioScience. 2016;66(8):666 - 682. doi:10.1093/biosci/biw077.
. Size of the local species pool determines invasibility of a C4-dominated grassland. Oikos. 2001;92:55 -61. doi:10.1034/j.1600-0706.2001.920107.x.
. Soil nutrient additions increase invertebrate herbivore abundances, but not herbivory, across three grassland systems. Oecologia. 2016;180(2):485 -497. doi:https://doi.org/10.1007/s00442-015-3471-7.
. Stoichiometric homeostasis predicts plant species dominance, temporal stability and responses to global change. Ecology. 2015;96(9):2335. doi:10.1890/14-1897.1.
. A test for community change using a null model approach. Ecological Applications. 2005;15:1761 -1771. doi:10.1890/04-1490.
A test of two mechanisms proposed to optimize grassland aboveground primary productivity in response to grazing. Journal of Plant Ecology. 2012;5:357 -365. doi:10.1093/jpe/rts020.
. Variation among biomes in temporal dynamics of aboveground primary production. Science. 2001;291:481 -484. doi:10.1126/science.291.5503.481.
Variation in gene expression of Andropogon gerardii in response to altered environmental conditions associated with climate change. Journal of Ecology. 2010;98:374 -383. doi:10.1111/j.1365-2745.2009.01618.x.
. Causes and consequences of species invasion and loss: the role of dominant species and diversity in maintaining ecosystem function. 2002;PhD Dissertation:1 -148.