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Global Change Biology · 2023 · Vol. 29 · Issue 23 · Wiley
Grassland and other herbaceous communities cover significant portions of Earth's terrestrial surface and provide many critical services, such as carbon sequestration, wildlife habitat, and food production. Forecasts of global change impacts on these services will require predictive tools, such as process‐based dynamic vegetation models. Yet, model representation of herbaceous communities and ecosystems lags substantially behin...
Global Change Biology · 2020 · Vol. 26 · Issue 3 · Wiley
Stem xylem‐specific hydraulic conductivity ( K S ) represents the potential for plant water transport normalized by xylem cross section, length, and driving force. Variation in K S has implications for plant transpiration and photosynthesis, growth and survival, and also the geographic distribution of species. Clarifying the global‐scale patterns of K S and its major drivers is needed to achieve a better understanding of how p...
Global Change Biology · 2018 · Vol. 24 · Issue 1 · Wiley
Numerous current efforts seek to improve the representation of ecosystem ecology and vegetation demographic processes within Earth System Models ( ESM s). These developments are widely viewed as an important step in developing greater realism in predictions of future ecosystem states and fluxes. Increased realism, however, leads to increased model complexity, with new features raising a suite of ecological questions that requi...
Global Change Biology · 2017 · Vol. 23 · Issue 6 · Wiley
Earth system models are incorporating plant trait diversity into their land components to better predict vegetation dynamics in a changing climate. However, extant plant trait distributions will not allow extrapolations to novel community assemblages in future climates, which will require a mechanistic understanding of the trade‐offs that determine trait diversity. In this study, we show how physiological trade‐offs involving...
Global Change Biology · 2013 · Vol. 19 · Issue 6 · Wiley
Predicted responses of transpiration to elevated atmospheric CO 2 concentration ( eCO 2 ) are highly variable amongst process‐based models. To better understand and constrain this variability amongst models, we conducted an intercomparison of 11 ecosystem models applied to data from two forest free‐air CO 2 enrichment ( FACE ) experiments at Duke University and Oak Ridge National Laboratory. We analysed model structures to ide...
Global Change Biology · 2008 · Vol. 14 · Issue 12 · Wiley
Global climate change is expected to result in a greater frequency of extreme weather, which can cause lag effects on aboveground net primary production (ANPP). However, our understanding of lag effects is limited. To explore lag effects following extreme weather, we applied four treatments (control, doubled precipitation, 4 °C warming, and warming plus doubled precipitation) for 1 year in a randomized block design and monitor...
Global Change Biology · 2008 · Vol. 14 · Issue 10 · Wiley
The ongoing changes in the global climate expose the world's ecosystems not only to increasing CO 2 concentrations and temperatures but also to altered precipitation ( P ) regimes. Using four well‐established process‐based ecosystem models (LPJ, DayCent, ORCHIDEE, TECO), we explored effects of potential P changes on water limitation and net primary production (NPP) in seven terrestrial ecosystems with distinctive vegetation ty...
Global Change Biology · 2008 · Vol. 14 · Issue 9 · Wiley
Interactive effects of multiple global change factors on ecosystem processes are complex. It is relatively expensive to explore those interactions in manipulative experiments. We conducted a modeling analysis to identify potentially important interactions and to stimulate hypothesis formulation for experimental research. Four models were used to quantify interactive effects of climate warming ( T ), altered precipitation amoun...