Browsing by Author "Zanne, Amy E"
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Item Functional traits and the growth-mortality tradeoff in tropical trees(Ecological Society of America, 2010) Wright, S Joseph; Kitajima, Kaoru; Kraft, Nathan J B; Reich, Peter B; Wright, Ian J; Bunker, Daniel E; Condit, Richard; Dalling, James W; Davies, Stuart J; Diaz, Sandra; Engelbrecht, Bettina M J; Harms, Kyle E; Hubbell, Stephen P; Marks, Christian O; Ruiz-Jaen, Maria C; Salvador, Cristina M; Zanne, Amy EA trade-off between growth and mortality rates characterizes tree species in closed canopy forests. This trade-off is maintained by inherent differences among species and spatial variation in light availability caused by canopy-opening disturbances. We evaluated conditions under which the trade-off is expressed and relationships with four key functional traits for 103 tree species from Barro Colorado Island, Panama. The trade-off is strongest for saplings for growth rates of the fastest growing individuals and mortality rates of the slowest growing individuals (r2 = 0.69), intermediate for saplings for average growth rates and overall mortality rates (r2 = 0.46), and much weaker for large trees (r2 ≤ 0.10). This parallels likely levels of spatial variation in light availability, which is greatest for fast- vs. slow-growing saplings and least for large trees with foliage in the forest canopy. Inherent attributes of species contributing to the trade-off include abilities to disperse, acquire resources, grow rapidly, and tolerate shade and other stresses. There is growing interest in the possibility that functional traits might provide insight into such ecological differences and a growing consensus that seed mass (SM), leaf mass per area (LMA), wood density (WD), and maximum height (Hmax) are key traits among forest trees. Seed mass, LMA, WD, and Hmax are predicted to be small for light-demanding species with rapid growth and mortality and large for shade-tolerant species with slow growth and mortality. Six of these trait–demographic rate predictions were realized for saplings; however, with the exception of WD, the relationships were weak (r2 < 0.1 for three and r2 < 0.2 for five of the six remaining relationships). The four traits together explained 43–44% of interspecific variation in species positions on the growth–mortality trade-off; however, WD alone accounted for >80% of the explained variation and, after WD was included, LMA and Hmax made insignificant contributions. Virtually the full range of values of SM, LMA, and Hmax occurred at all positions on the growth–mortality trade-off. Although WD provides a promising start, a successful trait-based ecology of tropical forest trees will require consideration of additional traits.Item The global spectrum of plant form and function(2016) Díaz, Sandra; Kattge, Jens; Cornelissen, Johannes H C; Wright, Ian J; Lavorel, Sandra; Dray, Stéphane; Reu, Björn; Kleyer, Michael; Wirth, Christian; Prentice, I. Colin; Garnier, Eric; Bönisch, Gerhard; Westoby, Mark; Poorter, Hendrik; Reich, Peter B; Moles, Angela T; Dickie, John; Gillison, Andrew N; Zanne, Amy E; Chave, Jérôme; Wright, S. Joseph; Sheremet’ev, Serge N; Jactel, Hervé; Baraloto, Christopher; Cerabolini, Bruno; Pierce, Simon; Shipley, Bill; Kirkup, Donald; Casanoves, Fernando; Joswig, Julia S; Günther, Angela; Falczuk, Valeria; Rüger, Nadja; Mahecha, Miguel D; Gorné, Lucas DEarth is home to a remarkable diversity of plant forms and life histories, yet comparatively few essential trait combinations have proved evolutionarily viable in today’s terrestrial biosphere. By analysing worldwide variation in six major traits critical to growth, survival and reproduction within the largest sample of vascular plant species ever compiled, we found that occupancy of six-dimensional trait space is strongly concentrated, indicating coordination and trade-offs. Three-quarters of trait variation is captured in a two-dimensional global spectrum of plant form and function. One major dimension within this plane reflects the size of whole plants and their parts; the other represents the leaf economics spectrum, which balances leaf construction costs against growth potential. The global plant trait spectrum provides a backdrop for elucidating constraints on evolution, for functionally qualifying species and ecosystems, and for improving models that predict future vegetation based on continuous variation in plant form and function.Item Supporting data for The hidden value of trees: Quantifying the ecosystem services of tree lineages and their major threats across the contiguous US(2021-06-29) Cavender-Bares, Jeannine; Nelson, Erik; Meireles, Jose Eduardo; Lasky, Jesse R; Miteva, Daniela A; Nowak, David; Pearse, William D; Helmus, Matthew; Zanne, Amy E; Fagan, William; Mihiar, Christopher; Muller, Nicholas Z; Kraft, Nathan; Polasky, Stephen; cavender@umn.edu; Cavender-Bares, JeannineTrees provide critical contributions to human well-being. They sequester and store greenhouse gasses, filter air pollutants, and provide wood, food, and other products, among other benefits. These benefits are threatened by climate change, fires, pests and pathogens. We show that the value of ecosystem services generated by US trees in forests, orchards, and plantations across five key services for which we had adequate data is $114 billion per annum (low: $85 B; high: $137 B; 2010 USD). The non-market ‘hidden’ ecosystem services of trees from carbon storage (51% of total value) and air pollution removal (37%) far exceed their commercial value from wood products and food crops (12%). The most valuable US tree species and lineages are also among those most threatened by known pests and pathogens, and the species most valuable for carbon storage are most at risk from increasing fire threat. Different species and lineages in different regions contribute to carbon storage and air pollution removal, which is distinct from tree crops that are often provided by the same species and lineages in different regions.Item Three keys to the radiation of angiosperms into freezing environments(Nature Publishing Group, 2014) Zanne, Amy E; Tank, David C; Cornwell, William K; Eastman, Jonathan M; Smith, Stephen A; FitzJohn, Richard G; McGlinn, Daniel J; O’Meara, Brian C; Moles, Angela T; Reich, Peter B; Royer, Dana L; Soltis, Douglas E; Stevens, Peter F; Westoby, Mark; Wright, Ian J; Aarssen, Lonnie; Bertin, Robert I; Calaminus, Andre; Govaerts, Rafaël; Hemmings, Frank; Leishman, Michelle R; Oleksyn, Jacek; Soltis, Pamela S; Swenson, Nathan G; Warman, Laura; Beaulieu, Jeremy MEarly flowering plants are thought to have been woody species restricted to warm habitats1, 2, 3. This lineage has since radiated into almost every climate, with manifold growth forms4. As angiosperms spread and climate changed, they evolved mechanisms to cope with episodic freezing. To explore the evolution of traits underpinning the ability to persist in freezing conditions, we assembled a large species-level database of growth habit (woody or herbaceous; 49,064 species), as well as leaf phenology (evergreen or deciduous), diameter of hydraulic conduits (that is, xylem vessels and tracheids) and climate occupancies (exposure to freezing). To model the evolution of species’ traits and climate occupancies, we combined these data with an unparalleled dated molecular phylogeny (32,223 species) for land plants. Here we show that woody clades successfully moved into freezing-prone environments by either possessing transport networks of small safe conduits5 and/or shutting down hydraulic function by dropping leaves during freezing. Herbaceous species largely avoided freezing periods by senescing cheaply constructed aboveground tissue. Growth habit has long been considered labile6, but we find that growth habit was less labile than climate occupancy. Additionally, freezing environments were largely filled by lineages that had already become herbs or, when remaining woody, already had small conduits (that is, the trait evolved before the climate occupancy). By contrast, most deciduous woody lineages had an evolutionary shift to seasonally shedding their leaves only after exposure to freezing (that is, the climate occupancy evolved before the trait). For angiosperms to inhabit novel cold environments they had to gain new structural and functional trait solutions; our results suggest that many of these solutions were probably acquired before their foray into the cold.