@article {KNZ002042, title = {Nutrients cause grassland biomass to outpace herbivory}, journal = {Nature Communications}, volume = {11}, year = {2020}, pages = {6036}, keywords = {LTER-KNZ}, doi = {10.1038/s41467-020-19870-y}, url = {http://www.nature.com/articles/s41467-020-19870-y}, author = {Borer, E. T. and Harpole, W. S. and Adler, P. B. and Arnillas, C. A. and Bugalho, M. N. and Cadotte, M. W. and Caldeira, M. C. and Campana, S. and Dickman, C. R. and Dickson, T. L. and Donohue, I. and Eskelinen, A. and Firn, J. L. and Graff, P. and Gruner, D. S. and Heckman, R. W. and Koltz, A. M. and Kimberly J. Komatsu and Lannes, L. S. and MacDougall, A. S. and Martina, J. P. and Moore, J. L. and Mortensen, B. and Ochoa-Hueso, R. and Olde Venterink, H. and Power, S. A. and Price, J. N. and Risch, A. C. and Sankaran, M. and sch{\"u}tz, M. and Sitters, J. and Stevens, C. J. and Virtanen, R. and Wilfahrt, P. A. and Seabloom, E. W.} } @article {KNZ001868, title = {Nutrient addition shifts plant community composition towards earlier flowering species in some prairie ecoregions in the U.S. Central Plains}, journal = {PLOS ONE}, year = {2017}, pages = {e0178440}, abstract = {

The distribution of flowering across the growing season is governed by each species\’ evolutionary history and climatic variability. However, global change factors, such as eutrophication and invasion, can alter plant community composition and thus change the distribution of flowering across the growing season. We examined three ecoregions (tall-, mixed, and short-grass prairie) across the U.S. Central Plains to determine how nutrient (nitrogen (N), phosphorus, and potassium (+micronutrient)) addition alters the temporal patterns of plant flowering traits. We calculated total community flowering potential (FP) by distributing peak-season plant cover values across the growing season, allocating each species\’ cover to only those months in which it typically flowers. We also generated separate FP profiles for exotic and native species and functional group. We compared the ability of the added nutrients to shift the distribution of these FP profiles (total and sub-groups) across the growing season. In all ecoregions, N increased the relative cover of both exotic species and C3 graminoids that flower in May through August. The cover of C4 graminoids decreased with added N, but the response varied by ecoregion and month. However, these functional changes only aggregated to shift the entire community\’s FP profile in the tall-grass prairie, where the relative cover of plants expected to flower in May and June increased and those that flower in September and October decreased with added N. The relatively low native cover in May and June may leave this ecoregion vulnerable to disturbance-induced invasion by exotic species that occupy this temporal niche. There was no change in the FP profile of the mixed and short-grass prairies with N addition as increased abundance of exotic species and C3 graminoids replaced other species that flower at the same time. In these communities a disturbance other than nutrient addition may be required to disrupt phenological patterns.

}, keywords = {LTER-KNZ}, doi = {10.1371/journal.pone.0178440}, url = {http://dx.plos.org/10.1371/journal.pone.0178440ttp}, author = {L.A. Biederman and Mortensen, B. and Fay, P.A. and Hagenah, N. and Knops, J. and Kimberly J. La Pierre and Laungani, R. and Lind, E. and McCulley, R. and Power, S. and Seabloom, E. and Tognetti, P.} } @article {KNZ001793, title = {Herbivores and nutrients control grassland plant diversity via light limitation}, journal = {Nature}, volume = {508}, year = {2014}, pages = {517 - 520}, keywords = {LTER-KNZ}, doi = {10.1038/nature13144}, url = {https://www.nature.com/articles/nature13144}, author = {E.T. Borer and Seabloom, E.W. and Gruner, D.S. and Harpole, W.S and Hillebrand, H. and Lind, E.M. and P. Adler and J. Alberti and Anderson, T.M. and J.D. Bakker and L.A. Biederman and D.M. Blumenthal and C.S. Brown and Brudvig, L.A. and Buckley, Y.M. and Cadotte, M. and Chu, C. and Cleland, E.E. and Crawley, M.J. and Daleo, P. and Damschen, E.I. and Davies, K.F. and DeCrappeo, N.M. and G. Du and Firn, J. and Hautier, Y. and Heckman, R.W. and Hector, A. and HilleRisLambers, J. and Iribarne, Oscar and Klein, J.A. and Knops, J.M.H. and Kimberly J. La Pierre and Leakey, A.D.B. and Li, W. and MacDougall, A.S. and McCulley, R.L. and Melbourne, B.A. and Mitchell, C.E. and Joslin L. Moore and Mortensen, B. and O{\textquoteright}Halloran, L.R. and Orrock, J.L. and Pascual, J. and Prober, S.M. and Pyke, D.A. and A. Risch and Schuetz, M. and M.D. Smith and Stevens, C.J. and L.L. Sullivan and Williams, R.J. and Wragg, P.D. and Wright, J.P. and Yang, L.H.} } @article {KNZ001791, title = {Life-history constraints in grassland plant species: a growth-defence trade-off is the norm}, journal = {Ecology Letters}, volume = {16}, year = {2013}, pages = {513 - 521}, abstract = {

Plant growth can be limited by resource acquisition and defence against consumers, leading to contrasting trade-off possibilities. The competition-defence hypothesis posits a trade-off between competitive ability and defence against enemies (e.g. herbivores and pathogens). The growth-defence hypothesis suggests that strong competitors for nutrients are also defended against enemies, at a cost to growth rate. We tested these hypotheses using observations of 706 plant populations of over 500 species before and following identical fertilisation and fencing treatments at 39 grassland sites worldwide. Strong positive covariance in species responses to both treatments provided support for a growth-defence trade-off: populations that increased with the removal of nutrient limitation (poor competitors) also increased following removal of consumers. This result held globally across 4 years within plant life-history groups and within the majority of individual sites. Thus, a growth-defence trade-off appears to be the norm, and mechanisms maintaining grassland biodiversity may operate within this constraint.

}, keywords = {LTER-KNZ}, doi = {10.1111/ele.12078}, url = {https://onlinelibrary.wiley.com/doi/abs/10.1111/ele.12078}, author = {Lind, E.M. and E.T. Borer and Seabloom, E. and P. Adler and J.D. Bakker and D.M. Blumenthal and Crawley, M. and Davies, K. and Firn, J. and Gruner, D.S. and Harpole, W.S. and Hautier, Y. and Hillebrand, H. and Knops, J. and Melbourne, B. and Mortensen, B. and A. Risch and Schuetz, M. and Stevens, C. and Wragg, P.D.} } @article {KNZ001790, title = {Predicting invasion in grassland ecosystems: is exotic dominance the real embarrassment of richness?}, journal = {Global Change Biology}, volume = {19}, year = {2013}, pages = {3677 - 3687}, abstract = {

Invasions have increased the size of regional species pools, but are typically assumed to reduce native diversity. However, global-scale tests of this assumption have been elusive because of the focus on exotic species richness, rather than relative abundance. This is problematic because low invader richness can indicate invasion resistance by the native community or, alternatively, dominance by a single exotic species. Here, we used a globally replicated study to quantify relationships between exotic richness and abundance in grass-dominated ecosystems in 13 countries on six continents, ranging from salt marshes to alpine tundra. We tested effects of human land use, native community diversity, herbivore pressure, and nutrient limitation on exotic plant dominance. Despite its widespread use, exotic richness was a poor proxy for exotic dominance at low exotic richness, because sites that contained few exotic species ranged from relatively pristine (low exotic richness and cover) to almost completely exotic-dominated ones (low exotic richness but high exotic cover). Both exotic cover and richness were predicted by native plant diversity (native grass richness) and land use (distance to cultivation). Although climate was important for predicting both exotic cover and richness, climatic factors predicting cover (precipitation variability) differed from those predicting richness (maximum temperature and mean temperature in the wettest quarter). Herbivory and nutrient limitation did not predict exotic richness or cover. Exotic dominance was greatest in areas with low native grass richness at the site- or regional-scale. Although this could reflect native grass displacement, a lack of biotic resistance is a more likely explanation, given that grasses comprise the most aggressive invaders. These findings underscore the need to move beyond richness as a surrogate for the extent of invasion, because this metric confounds monodominance with invasion resistance. Monitoring species\&$\#$39; relative abundance will more rapidly advance our understanding of invasions.

}, keywords = {LTER-KNZ}, doi = {10.1111/gcb.12370}, url = {https://onlinelibrary.wiley.com/doi/abs/10.1111/gcb.12370}, author = {Seabloom, E.W. and E.T. Borer and Buckley, Y. and Cleland, E.E. and Davies, K. and Firn, J. and Harpole, W.S. and Hautier, Y. and Lind, E. and MacDougall, A. and Orrock, J.L. and Prober, S.M. and P. Adler and J. Alberti and Anderson, M.T. and J.D. Bakker and L.A. Biederman and D.M. Blumenthal and C.S. Brown and Brudvig, L.A. and Caldeira, M. and Chu, C. and Crawley, M.J. and Daleo, P. and Damschen, E.I. and D{\textquoteright}Antonio, C.M. and DeCrappeo, N.M. and Dickman, C.R. and G. Du and Fay, P.A. and Frater, P. and Gruner, D.S. and Hagenah, N. and Hector, A. and Helm, A. and Hillebrand, H. and Hofmockel, K.S. and Humphries, H.C. and Iribarne, O. and Jin, V.L. and Kay, A. and Kirkman, K.P. and Klein, J.A. and Knops, J.M.H. and Kimberly J. La Pierre and L. Ladwig and Lambrinos, J.G. and Leakey, A.D.B. and Li, Q. and Li, W. and McCulley, R. and Melbourne, B. and Mitchell, C.E. and Joslin L. Moore and J.W. Morgan and Mortensen, B. and O{\textquoteright}Halloran, L.R. and P{\"a}rtel, M. and Pascual, J and Pyke, D.A. and A. Risch and Salguero-Gomez, R. and Sankaran, M. and Schuetz, M. and Simonsen, A. and M.D. Smith and Stevens, C. and Sullivan, L. and Wardle, G.M. and Wolkovich, E.M. and Wragg, P.D. and Wright, J. and Yang, L.} }