Konza LTER Publications
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Increased precipitation event size increases aboveground net primary productivity in a semi-arid grassland. Oecologia. 2008;158:129 -140. doi:10.1007/s00442-008-1116-9.
. Increased photosynthesis and water potentials in Silphium integrifolium galled by cynipid wasps. Oecologia. 1993;93:114 -120. doi:10.1007/BF00321200.
. Impacts of plant diversity on arthropod communities and plant-herbivore network architecture. Ecosphere. 2017;8(10):e01983. doi:10.1002/ecs2.1983.
. The immediate and prolonged effects of climate extremes on soil respiration in a mesic grassland. Journal of Geophysical Research: Biogeosciences. 2016;121(4):1034 - 1044. doi:10.1002/2015JG003256.
. Identifying the water sources consumed by bison: implications for large mammalian grazers worldwide. Ecosphere. 2013;4:23 -. doi:10.1890/ES12-00359.1.
. Hymenolepis ackerti n. sp. (Eucestoda: Hymenolepididae) infecting cricetid rodents from the central Great Plains of North America. Revista Mexicana de Biodiversidad. 2023;94:e944927. doi:10.22201/ib.20078706e.2023.94.4927.
. How long do population level field experiments need to be? Utilising data from the 40‐year‐old LTER network. . Ecology Letters. 2021;24(5):1103 - 1111. doi:10.1111/ele.v24.510.1111/ele.13710.
. How long do population level field experiments need to be? Utilising data from the 40‐year‐old LTER network. . Ecology Letters. 2021;24(5):1103 - 1111. doi:10.1111/ele.v24.510.1111/ele.13710.
. How landscape heterogeneity governs stream water concentration-discharge behavior in carbonate terrains (Konza Prairie, USA). Chemical Geology. 2019;527(20):118989. doi:10.1016/j.chemgeo.2018.12.002.
. How do extra nutrients affect the timing of flowering in prairies. Environmental Science Journal for Teens. 2017;(September, 2017). Available at: http://www.sciencejournalforkids.org/uploads/5/4/2/8/54289603/flowers_article.pdf.
Host plant species effects on arbuscular mycorrhizal fungal communities in tallgrass prairie. Oecologia. 2000;122:435 -444. doi:10.1007/s004420050050.
. History and use of Konza Prairie Research Natural Area. The Prairie Scout. 1985;5:63 -95.
. High-throughput amplicon sequencing of rRNA genes requires a copy number correction to accurately reflect the effects of management practices on soil nematode community structure. Molecular Ecology. 2013;22:5456 -5471. doi:10.1111/mec.12480.
. Higher-order bud production increases tillering capacity in the perennial caespitose grass Scribner's Panicum (Dichanthelium oligosanthes). Botany. 2012;90:884 -890. doi:10.1139/b2012-043.
. High propagule production and reproductive fitness homeostasis contribute to the invasiveness of Lespedeza cuneata (Fabaceae). Biological Invasions. 2009;11:1913 -1927. doi:10.1007/s10530-008-9369-0.
. High levels of relatedness between Brown-headed Cowbird (Molothrus ater) nestmates in a heavily parasitized host community. The Auk. 2012;129:623 -631. doi:10.1525/auk.2012.11236.
. Herpetofauna of the Konza Prairie Research Natural Area, Kansas. The Prairie Naturalist. 1985;17:101 -112.
. Herbivores and nutrients control grassland plant diversity via light limitation. Nature. 2014;508(7497):517 - 520. doi:10.1038/nature13144.
Herbivores and nutrients control grassland plant diversity via light limitation. Nature. 2014;508(7497):517 - 520. doi:10.1038/nature13144.
Herbivores and nutrients control grassland plant diversity via light limitation. Nature. 2014;508(7497):517 - 520. doi:10.1038/nature13144.
Herbivores and nutrients control grassland plant diversity via light limitation. Nature. 2014;508(7497):517 - 520. doi:10.1038/nature13144.
Herbivores and nutrients control grassland plant diversity via light limitation. Nature. 2014;508(7497):517 - 520. doi:10.1038/nature13144.
Herbivores and nutrients control grassland plant diversity via light limitation. Nature. 2014;508(7497):517 - 520. doi:10.1038/nature13144.
Harmony on the prairie? Grassland plant and animal community responses to variation in climate across land‐use gradients. Ecology. 2020;101(5):e02986. doi:10.1002/ecy.2986.
Grazing management effects on plant species diversity in tallgrass prairie. Journal of Range Management. 2004;57:58 -65. doi:10.2111/1551-5028(2004)057[0058:GMEOPS]2.0.CO;2.
. Grazing management effects on plant species diversity in tallgrass prairie. Journal of Range Management. 2004;57:58 -65. doi:10.2111/1551-5028(2004)057[0058:GMEOPS]2.0.CO;2.
. Grassland woody encroachment alters subsurface mineral weathering and groundwater composition in a carbonate system. Chemical Geology. 2025;673. doi:10.1016/j.chemgeo.2024.122522.
Grassland sensitivity to drought is related to functional composition across East Asia and North America. Ecology. 2024;105(2):e4220. doi:10.1002/ecy.4220.
Grassland productivity limited by multiple nutrients. Nature Plants. 2015;1(7):15080. doi:10.1038/nplants.2015.80.
Grassland productivity limited by multiple nutrients. Nature Plants. 2015;1(7):15080. doi:10.1038/nplants.2015.80.
Grassland productivity limited by multiple nutrients. Nature Plants. 2015;1(7):15080. doi:10.1038/nplants.2015.80.
Grassland productivity limited by multiple nutrients. Nature Plants. 2015;1(7):15080. doi:10.1038/nplants.2015.80.
Grass evolutionary lineages can be identified using hyperspectral leaf reflectance. Journal of Geophysical Research: Biogeosciences. 2024;129(2):e2023JG007852. doi:10.1029/2023JG007852.
Grass evolutionary lineages can be identified using hyperspectral leaf reflectance. Journal of Geophysical Research: Biogeosciences. 2024;129(2):e2023JG007852. doi:10.1029/2023JG007852.
Gradient models, gradient analysis and hierarchical structure in plant communities. Oikos. 1997;78:23 -30. doi:10.2307/3545796.
. Glomus Mortonii sp. Nov., a previously undescribed species in the Glomaceae isolated from the tallgrass prairie in Kansas. Mycotoxon. 1991;42:9 -15.
. Global-scale similarities in nitrogen release patterns during long-term decomposition. Science. 2007;315:361 -364. doi:10.1126/science.1134853.
Global-scale similarities in nitrogen release patterns during long-term decomposition. Science. 2007;315:361 -364. doi:10.1126/science.1134853.
Global synthesis of the temperature sensitivity of leaf litter breakdown in streams and rivers. Global Change Biology. 2017;23(8):3064-3075. doi:10.1111/gcb.13609.
Global patterns and drivers of ecosystem functioning in rivers and riparian zones. Science Advances. 2019;5(1):eaav0486. doi:10.1126/sciadv.aav0486.
Global patterns and drivers of ecosystem functioning in rivers and riparian zones. Science Advances. 2019;5(1):eaav0486. doi:10.1126/sciadv.aav0486.
Global patterns and drivers of ecosystem functioning in rivers and riparian zones. Science Advances. 2019;5(1):eaav0486. doi:10.1126/sciadv.aav0486.
Global patterns and drivers of ecosystem functioning in rivers and riparian zones. Science Advances. 2019;5(1):eaav0486. doi:10.1126/sciadv.aav0486.
Global patterns and drivers of ecosystem functioning in rivers and riparian zones. Science Advances. 2019;5(1):eaav0486. doi:10.1126/sciadv.aav0486.
Global impacts of fertilization and herbivore removal on soil net nitrogen mineralization are modulated by local climate and soil properties. Global Change Biology. 2020;26(12). doi:10.1111/gcb.15308.
Global change effects on plant communities are magnified by time and the number of global change factors imposed. Proceedings of the National Academy of Sciences. 2019;116(36):17867-17873. doi:10.1073/pnas.1819027116.
Global change effects on plant communities are magnified by time and the number of global change factors imposed. Proceedings of the National Academy of Sciences. 2019;116(36):17867-17873. doi:10.1073/pnas.1819027116.
Global change effects on plant communities are magnified by time and the number of global change factors imposed. Proceedings of the National Academy of Sciences. 2019;116(36):17867-17873. doi:10.1073/pnas.1819027116.
Global change effects on plant communities are magnified by time and the number of global change factors imposed. Proceedings of the National Academy of Sciences. 2019;116(36):17867-17873. doi:10.1073/pnas.1819027116.
Global change effects on plant communities are magnified by time and the number of global change factors imposed. Proceedings of the National Academy of Sciences. 2019;116(36):17867-17873. doi:10.1073/pnas.1819027116.